WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.7128906A>C | CA403671778 | INSR | c.2891T>G (p.Phe964Cys) c.2855T>G (p.Phe952Cys) c.2966T>G (p.Phe989Cys) c.2930T>G (p.Phe977Cys) c.2888T>G (p.Phe963Cys) c.2852T>G (p.Phe951Cys) | |
| 19 | g.7128906A>G | CA403671779 | INSR | c.2891T>C (p.Phe964Ser) c.2855T>C (p.Phe952Ser) c.2966T>C (p.Phe989Ser) c.2930T>C (p.Phe977Ser) c.2888T>C (p.Phe963Ser) c.2852T>C (p.Phe951Ser) | |
| 19 | g.7128906A>T | CA403671780 | INSR | c.2891T>A (p.Phe964Tyr) c.2855T>A (p.Phe952Tyr) c.2966T>A (p.Phe989Tyr) c.2930T>A (p.Phe977Tyr) c.2888T>A (p.Phe963Tyr) c.2852T>A (p.Phe951Tyr) | |
| 19 | g.7128907A>C | CA403671781 | INSR | c.2890T>G (p.Phe964Val) c.2854T>G (p.Phe952Val) c.2965T>G (p.Phe989Val) c.2929T>G (p.Phe977Val) c.2887T>G (p.Phe963Val) c.2851T>G (p.Phe951Val) | |
| 19 | g.7128907A>G | CA403671782 | INSR | c.2890T>C (p.Phe964Leu) c.2854T>C (p.Phe952Leu) c.2965T>C (p.Phe989Leu) c.2929T>C (p.Phe977Leu) c.2887T>C (p.Phe963Leu) c.2851T>C (p.Phe951Leu) | |
| 19 | g.7128907A>T | CA403671783 | INSR | c.2890T>A (p.Phe964Ile) c.2854T>A (p.Phe952Ile) c.2965T>A (p.Phe989Ile) c.2929T>A (p.Phe977Ile) c.2887T>A (p.Phe963Ile) c.2851T>A (p.Phe951Ile) | |
| 19 | g.7128908G>A | CA9135419 | INSR | c.2889C>T (p.Ile963=) c.2853C>T (p.Ile951=) c.2964C>T (p.Ile988=) c.2928C>T (p.Ile976=) c.2886C>T (p.Ile962=) c.2850C>T (p.Ile950=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7128908G>C | CA403671784 | INSR | c.2889C>G (p.Ile963Met) c.2853C>G (p.Ile951Met) c.2964C>G (p.Ile988Met) c.2928C>G (p.Ile976Met) c.2886C>G (p.Ile962Met) c.2850C>G (p.Ile950Met) | |
| 19 | g.7128908G= | CA2320769471 | INSR | c.2889C= (p.Ile963=) c.2853C= (p.Ile951=) c.2964C= (p.Ile988=) c.2928C= (p.Ile976=) c.2886C= (p.Ile962=) c.2850C= (p.Ile950=) | |
| 19 | g.7128908G>T | CA505217398 | INSR | c.2889C>A (p.Ile963=) c.2853C>A (p.Ile951=) c.2964C>A (p.Ile988=) c.2928C>A (p.Ile976=) c.2886C>A (p.Ile962=) c.2850C>A (p.Ile950=) | |
| 19 | g.7128909A= | CA2320769472 | INSR | c.2888T= (p.Ile963=) c.2852T= (p.Ile951=) c.2963T= (p.Ile988=) c.2927T= (p.Ile976=) c.2885T= (p.Ile962=) c.2849T= (p.Ile950=) | |
| 19 | g.7128909A>C | CA403671785 | INSR | c.2888T>G (p.Ile963Ser) c.2852T>G (p.Ile951Ser) c.2963T>G (p.Ile988Ser) c.2927T>G (p.Ile976Ser) c.2885T>G (p.Ile962Ser) c.2849T>G (p.Ile950Ser) | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.7128909A>G | CA403671786 | INSR | c.2888T>C (p.Ile963Thr) c.2852T>C (p.Ile951Thr) c.2963T>C (p.Ile988Thr) c.2927T>C (p.Ile976Thr) c.2885T>C (p.Ile962Thr) c.2849T>C (p.Ile950Thr) | |
| 19 | g.7128909A>T | CA403671787 | INSR | c.2888T>A (p.Ile963Asn) c.2852T>A (p.Ile951Asn) c.2963T>A (p.Ile988Asn) c.2927T>A (p.Ile976Asn) c.2885T>A (p.Ile962Asn) c.2849T>A (p.Ile950Asn) | |
| 19 | g.7128910T>A | CA403671789 | INSR | c.2887A>T (p.Ile963Phe) c.2851A>T (p.Ile951Phe) c.2962A>T (p.Ile988Phe) c.2926A>T (p.Ile976Phe) c.2884A>T (p.Ile962Phe) c.2848A>T (p.Ile950Phe) | |
| 19 | g.7128910T>C | CA403671790 | INSR | c.2887A>G (p.Ile963Val) c.2851A>G (p.Ile951Val) c.2962A>G (p.Ile988Val) c.2926A>G (p.Ile976Val) c.2884A>G (p.Ile962Val) c.2848A>G (p.Ile950Val) | |
| 19 | g.7128910T>G | CA403671788 | INSR | c.2887A>C (p.Ile963Leu) c.2851A>C (p.Ile951Leu) c.2962A>C (p.Ile988Leu) c.2926A>C (p.Ile976Leu) c.2884A>C (p.Ile962Leu) c.2848A>C (p.Ile950Leu) | |
| 19 | g.7128911G>A | CA505217399 | INSR | c.2886C>T (p.Leu962=) c.2850C>T (p.Leu950=) c.2961C>T (p.Leu987=) c.2925C>T (p.Leu975=) c.2883C>T (p.Leu961=) c.2847C>T (p.Leu949=) | gnomAD v4 |
| 19 | g.7128911G>C | CA505217400 | INSR | c.2886C>G (p.Leu962=) c.2850C>G (p.Leu950=) c.2961C>G (p.Leu987=) c.2925C>G (p.Leu975=) c.2883C>G (p.Leu961=) c.2847C>G (p.Leu949=) | |
| 19 | g.7128911G>T | CA505217401 | INSR | c.2886C>A (p.Leu962=) c.2850C>A (p.Leu950=) c.2961C>A (p.Leu987=) c.2925C>A (p.Leu975=) c.2883C>A (p.Leu961=) c.2847C>A (p.Leu949=) | |
| 19 | g.7128912A>C | CA403671793 | INSR | c.2885T>G (p.Leu962Arg) c.2849T>G (p.Leu950Arg) c.2960T>G (p.Leu987Arg) c.2924T>G (p.Leu975Arg) c.2882T>G (p.Leu961Arg) c.2846T>G (p.Leu949Arg) | |
| 19 | g.7128912A>G | CA403671791 | INSR | c.2885T>C (p.Leu962Pro) c.2849T>C (p.Leu950Pro) c.2960T>C (p.Leu987Pro) c.2924T>C (p.Leu975Pro) c.2882T>C (p.Leu961Pro) c.2846T>C (p.Leu949Pro) | |
| 19 | g.7128912A>T | CA403671792 | INSR | c.2885T>A (p.Leu962His) c.2849T>A (p.Leu950His) c.2960T>A (p.Leu987His) c.2924T>A (p.Leu975His) c.2882T>A (p.Leu961His) c.2846T>A (p.Leu949His) | |
| 19 | g.7128913G>A | CA403671794 | INSR | c.2884C>T (p.Leu962Phe) c.2848C>T (p.Leu950Phe) c.2959C>T (p.Leu987Phe) c.2923C>T (p.Leu975Phe) c.2881C>T (p.Leu961Phe) c.2845C>T (p.Leu949Phe) | |
| 19 | g.7128913G>C | CA403671795 | INSR | c.2884C>G (p.Leu962Val) c.2848C>G (p.Leu950Val) c.2959C>G (p.Leu987Val) c.2923C>G (p.Leu975Val) c.2881C>G (p.Leu961Val) c.2845C>G (p.Leu949Val) | |
| 19 | g.7128913G>T | CA403671796 | INSR | c.2884C>A (p.Leu962Ile) c.2848C>A (p.Leu950Ile) c.2959C>A (p.Leu987Ile) c.2923C>A (p.Leu975Ile) c.2881C>A (p.Leu961Ile) c.2845C>A (p.Leu949Ile) | |
| 19 | g.7128914G>A | CA505217402 | INSR | c.2883C>T (p.Pro961=) c.2847C>T (p.Pro949=) c.2958C>T (p.Pro986=) c.2922C>T (p.Pro974=) c.2880C>T (p.Pro960=) c.2844C>T (p.Pro948=) | |
| 19 | g.7128914G>C | CA505217403 | INSR | c.2883C>G (p.Pro961=) c.2847C>G (p.Pro949=) c.2958C>G (p.Pro986=) c.2922C>G (p.Pro974=) c.2880C>G (p.Pro960=) c.2844C>G (p.Pro948=) | gnomAD v4 |
| 19 | g.7128914G= | CA2320769473 | INSR | c.2883C= (p.Pro961=) c.2847C= (p.Pro949=) c.2958C= (p.Pro986=) c.2922C= (p.Pro974=) c.2880C= (p.Pro960=) c.2844C= (p.Pro948=) | |
| 19 | g.7128914G>T | CA505217404 | INSR | c.2883C>A (p.Pro961=) c.2847C>A (p.Pro949=) c.2958C>A (p.Pro986=) c.2922C>A (p.Pro974=) c.2880C>A (p.Pro960=) c.2844C>A (p.Pro948=) | dbSNP gnomAD v3 gnomAD v4 |
| 19 | g.7128915G>A | CA403671799 | INSR | c.2882C>T (p.Pro961Leu) c.2846C>T (p.Pro949Leu) c.2957C>T (p.Pro986Leu) c.2921C>T (p.Pro974Leu) c.2879C>T (p.Pro960Leu) c.2843C>T (p.Pro948Leu) | |
| 19 | g.7128915G>C | CA403671798 | INSR | c.2882C>G (p.Pro961Arg) c.2846C>G (p.Pro949Arg) c.2957C>G (p.Pro986Arg) c.2921C>G (p.Pro974Arg) c.2879C>G (p.Pro960Arg) c.2843C>G (p.Pro948Arg) | |
| 19 | g.7128915G>T | CA403671797 | INSR | c.2882C>A (p.Pro961His) c.2846C>A (p.Pro949His) c.2957C>A (p.Pro986His) c.2921C>A (p.Pro974His) c.2879C>A (p.Pro960His) c.2843C>A (p.Pro948His) | |
| 19 | g.7128916G>A | CA403671800 | INSR | c.2881C>T (p.Pro961Ser) c.2845C>T (p.Pro949Ser) c.2956C>T (p.Pro986Ser) c.2920C>T (p.Pro974Ser) c.2878C>T (p.Pro960Ser) c.2842C>T (p.Pro948Ser) | COSMIC |
| 19 | g.7128916G>C | CA403671801 | INSR | c.2881C>G (p.Pro961Ala) c.2845C>G (p.Pro949Ala) c.2956C>G (p.Pro986Ala) c.2920C>G (p.Pro974Ala) c.2878C>G (p.Pro960Ala) c.2842C>G (p.Pro948Ala) | |
| 19 | g.7128916G>T | CA403671802 | INSR | c.2881C>A (p.Pro961Thr) c.2845C>A (p.Pro949Thr) c.2956C>A (p.Pro986Thr) c.2920C>A (p.Pro974Thr) c.2878C>A (p.Pro960Thr) c.2842C>A (p.Pro948Thr) | |
| 19 | g.7128917G>A | CA505217405 | INSR | c.2880C>T (p.Gly960=) c.2844C>T (p.Gly948=) c.2955C>T (p.Gly985=) c.2919C>T (p.Gly973=) c.2877C>T (p.Gly959=) c.2841C>T (p.Gly947=) | |
| 19 | g.7128917G>C | CA505217406 | INSR | c.2880C>G (p.Gly960=) c.2844C>G (p.Gly948=) c.2955C>G (p.Gly985=) c.2919C>G (p.Gly973=) c.2877C>G (p.Gly959=) c.2841C>G (p.Gly947=) | gnomAD v4 |
| 19 | g.7128917G>T | CA505217407 | INSR | c.2880C>A (p.Gly960=) c.2844C>A (p.Gly948=) c.2955C>A (p.Gly985=) c.2919C>A (p.Gly973=) c.2877C>A (p.Gly959=) c.2841C>A (p.Gly947=) | gnomAD v4 |
| 19 | g.7128918C>A | CA403671803 | INSR | c.2879G>T (p.Gly960Val) c.2843G>T (p.Gly948Val) c.2954G>T (p.Gly985Val) c.2918G>T (p.Gly973Val) c.2876G>T (p.Gly959Val) c.2840G>T (p.Gly947Val) | |
| 19 | g.7128918C>G | CA403671804 | INSR | c.2879G>C (p.Gly960Ala) c.2843G>C (p.Gly948Ala) c.2954G>C (p.Gly985Ala) c.2918G>C (p.Gly973Ala) c.2876G>C (p.Gly959Ala) c.2840G>C (p.Gly947Ala) | |
| 19 | g.7128918C>T | CA403671805 | INSR | c.2879G>A (p.Gly960Asp) c.2843G>A (p.Gly948Asp) c.2954G>A (p.Gly985Asp) c.2918G>A (p.Gly973Asp) c.2876G>A (p.Gly959Asp) c.2840G>A (p.Gly947Asp) | gnomAD v4 |
| 19 | g.7128919C>A | CA403671807 | INSR | c.2878G>T (p.Gly960Cys) c.2842G>T (p.Gly948Cys) c.2953G>T (p.Gly985Cys) c.2917G>T (p.Gly973Cys) c.2875G>T (p.Gly959Cys) c.2839G>T (p.Gly947Cys) | |
| 19 | g.7128919C= | CA2320769474 | INSR | c.2878G= (p.Gly960=) c.2842G= (p.Gly948=) c.2953G= (p.Gly985=) c.2917G= (p.Gly973=) c.2875G= (p.Gly959=) c.2839G= (p.Gly947=) | |
| 19 | g.7128919C>G | CA403671806 | INSR | c.2878G>C (p.Gly960Arg) c.2842G>C (p.Gly948Arg) c.2953G>C (p.Gly985Arg) c.2917G>C (p.Gly973Arg) c.2875G>C (p.Gly959Arg) c.2839G>C (p.Gly947Arg) | |
| 19 | g.7128919C>T | CA9135420 | INSR | c.2878G>A (p.Gly960Ser) c.2842G>A (p.Gly948Ser) c.2953G>A (p.Gly985Ser) c.2917G>A (p.Gly973Ser) c.2875G>A (p.Gly959Ser) c.2839G>A (p.Gly947Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 19 | g.7128920G>A | CA9135421 | INSR | c.2877C>T (p.Ile959=) c.2841C>T (p.Ile947=) c.2952C>T (p.Ile984=) c.2916C>T (p.Ile972=) c.2874C>T (p.Ile958=) c.2838C>T (p.Ile946=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.7128920G>C | CA403671808 | INSR | c.2877C>G (p.Ile959Met) c.2841C>G (p.Ile947Met) c.2952C>G (p.Ile984Met) c.2916C>G (p.Ile972Met) c.2874C>G (p.Ile958Met) c.2838C>G (p.Ile946Met) | |
| 19 | g.7128920G= | CA2320769475 | INSR | c.2877C= (p.Ile959=) c.2841C= (p.Ile947=) c.2952C= (p.Ile984=) c.2916C= (p.Ile972=) c.2874C= (p.Ile958=) c.2838C= (p.Ile946=) | |
| 19 | g.7128920G>T | CA505217408 | INSR | c.2877C>A (p.Ile959=) c.2841C>A (p.Ile947=) c.2952C>A (p.Ile984=) c.2916C>A (p.Ile972=) c.2874C>A (p.Ile958=) c.2838C>A (p.Ile946=) |