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.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=) | |
| 19 | g.7128921A>C | CA403671809 | INSR | c.2876T>G (p.Ile959Ser) c.2840T>G (p.Ile947Ser) c.2951T>G (p.Ile984Ser) c.2915T>G (p.Ile972Ser) c.2873T>G (p.Ile958Ser) c.2837T>G (p.Ile946Ser) | |
| 19 | g.7128921A>G | CA403671810 | INSR | c.2876T>C (p.Ile959Thr) c.2840T>C (p.Ile947Thr) c.2951T>C (p.Ile984Thr) c.2915T>C (p.Ile972Thr) c.2873T>C (p.Ile958Thr) c.2837T>C (p.Ile946Thr) | |
| 19 | g.7128921A>T | CA403671811 | INSR | c.2876T>A (p.Ile959Asn) c.2840T>A (p.Ile947Asn) c.2951T>A (p.Ile984Asn) c.2915T>A (p.Ile972Asn) c.2873T>A (p.Ile958Asn) c.2837T>A (p.Ile946Asn) | |
| 19 | g.7128922T>A | CA403671812 | INSR | c.2875A>T (p.Ile959Phe) c.2839A>T (p.Ile947Phe) c.2950A>T (p.Ile984Phe) c.2914A>T (p.Ile972Phe) c.2872A>T (p.Ile958Phe) c.2836A>T (p.Ile946Phe) | |
| 19 | g.7128922T>C | CA403671813 | INSR | c.2875A>G (p.Ile959Val) c.2839A>G (p.Ile947Val) c.2950A>G (p.Ile984Val) c.2914A>G (p.Ile972Val) c.2872A>G (p.Ile958Val) c.2836A>G (p.Ile946Val) | |
| 19 | g.7128922T>G | CA403671814 | INSR | c.2875A>C (p.Ile959Leu) c.2839A>C (p.Ile947Leu) c.2950A>C (p.Ile984Leu) c.2914A>C (p.Ile972Leu) c.2872A>C (p.Ile958Leu) c.2836A>C (p.Ile946Leu) | |
| 19 | g.7128923G>A | CA505217409 | INSR | c.2874C>T (p.Ile958=) c.2838C>T (p.Ile946=) c.2949C>T (p.Ile983=) c.2913C>T (p.Ile971=) c.2871C>T (p.Ile957=) c.2835C>T (p.Ile945=) | |
| 19 | g.7128923G>C | CA403671815 | INSR | c.2874C>G (p.Ile958Met) c.2838C>G (p.Ile946Met) c.2949C>G (p.Ile983Met) c.2913C>G (p.Ile971Met) c.2871C>G (p.Ile957Met) c.2835C>G (p.Ile945Met) | |
| 19 | g.7128923G>T | CA505217410 | INSR | c.2874C>A (p.Ile958=) c.2838C>A (p.Ile946=) c.2949C>A (p.Ile983=) c.2913C>A (p.Ile971=) c.2871C>A (p.Ile957=) c.2835C>A (p.Ile945=) | gnomAD v4 |
| 19 | g.7128924A>C | CA403671816 | INSR | c.2873T>G (p.Ile958Ser) c.2837T>G (p.Ile946Ser) c.2948T>G (p.Ile983Ser) c.2912T>G (p.Ile971Ser) c.2870T>G (p.Ile957Ser) c.2834T>G (p.Ile945Ser) | |
| 19 | g.7128924A>G | CA403671817 | INSR | c.2873T>C (p.Ile958Thr) c.2837T>C (p.Ile946Thr) c.2948T>C (p.Ile983Thr) c.2912T>C (p.Ile971Thr) c.2870T>C (p.Ile957Thr) c.2834T>C (p.Ile945Thr) | |
| 19 | g.7128924A>T | CA403671818 | INSR | c.2873T>A (p.Ile958Asn) c.2837T>A (p.Ile946Asn) c.2948T>A (p.Ile983Asn) c.2912T>A (p.Ile971Asn) c.2870T>A (p.Ile957Asn) c.2834T>A (p.Ile945Asn) | |
| 19 | g.7128925T>A | CA403671819 | INSR | c.2872A>T (p.Ile958Phe) c.2836A>T (p.Ile946Phe) c.2947A>T (p.Ile983Phe) c.2911A>T (p.Ile971Phe) c.2869A>T (p.Ile957Phe) c.2833A>T (p.Ile945Phe) | |
| 19 | g.7128925T>C | CA9135422 | INSR | c.2872A>G (p.Ile958Val) c.2836A>G (p.Ile946Val) c.2947A>G (p.Ile983Val) c.2911A>G (p.Ile971Val) c.2869A>G (p.Ile957Val) c.2833A>G (p.Ile945Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.7128925T>G | CA403671820 | INSR | c.2872A>C (p.Ile958Leu) c.2836A>C (p.Ile946Leu) c.2947A>C (p.Ile983Leu) c.2911A>C (p.Ile971Leu) c.2869A>C (p.Ile957Leu) c.2833A>C (p.Ile945Leu) | |
| 19 | g.7128925T= | CA2320769476 | INSR | c.2872A= (p.Ile958=) c.2836A= (p.Ile946=) c.2947A= (p.Ile983=) c.2911A= (p.Ile971=) c.2869A= (p.Ile957=) c.2833A= (p.Ile945=) | |
| 19 | g.7128926A= | CA2320769477 | INSR | c.2871T= (p.Ile957=) c.2835T= (p.Ile945=) c.2946T= (p.Ile982=) c.2910T= (p.Ile970=) c.2868T= (p.Ile956=) c.2832T= (p.Ile944=) |