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.7128899A>C | CA403671763 | INSR | c.2898T>G (p.Phe966Leu) c.2862T>G (p.Phe954Leu) c.2973T>G (p.Phe991Leu) c.2937T>G (p.Phe979Leu) c.2895T>G (p.Phe965Leu) c.2859T>G (p.Phe953Leu) | |
| 19 | g.7128899A>G | CA505217392 | INSR | c.2898T>C (p.Phe966=) c.2862T>C (p.Phe954=) c.2973T>C (p.Phe991=) c.2937T>C (p.Phe979=) c.2895T>C (p.Phe965=) c.2859T>C (p.Phe953=) | |
| 19 | g.7128899A>T | CA403671764 | INSR | c.2898T>A (p.Phe966Leu) c.2862T>A (p.Phe954Leu) c.2973T>A (p.Phe991Leu) c.2937T>A (p.Phe979Leu) c.2895T>A (p.Phe965Leu) c.2859T>A (p.Phe953Leu) | |
| 19 | g.7128900A>C | CA403671765 | INSR | c.2897T>G (p.Phe966Cys) c.2861T>G (p.Phe954Cys) c.2972T>G (p.Phe991Cys) c.2936T>G (p.Phe979Cys) c.2894T>G (p.Phe965Cys) c.2858T>G (p.Phe953Cys) | |
| 19 | g.7128900A>G | CA403671766 | INSR | c.2897T>C (p.Phe966Ser) c.2861T>C (p.Phe954Ser) c.2972T>C (p.Phe991Ser) c.2936T>C (p.Phe979Ser) c.2894T>C (p.Phe965Ser) c.2858T>C (p.Phe953Ser) | |
| 19 | g.7128900A>T | CA403671767 | INSR | c.2897T>A (p.Phe966Tyr) c.2861T>A (p.Phe954Tyr) c.2972T>A (p.Phe991Tyr) c.2936T>A (p.Phe979Tyr) c.2894T>A (p.Phe965Tyr) c.2858T>A (p.Phe953Tyr) | |
| 19 | g.7128901A= | CA2320769469 | INSR | c.2896T= (p.Phe966=) c.2860T= (p.Phe954=) c.2971T= (p.Phe991=) c.2935T= (p.Phe979=) c.2893T= (p.Phe965=) c.2857T= (p.Phe953=) | |
| 19 | g.7128901A>C | CA403671768 | INSR | c.2896T>G (p.Phe966Val) c.2860T>G (p.Phe954Val) c.2971T>G (p.Phe991Val) c.2935T>G (p.Phe979Val) c.2893T>G (p.Phe965Val) c.2857T>G (p.Phe953Val) | |
| 19 | g.7128901A>G | CA403671769 | INSR | c.2896T>C (p.Phe966Leu) c.2860T>C (p.Phe954Leu) c.2971T>C (p.Phe991Leu) c.2935T>C (p.Phe979Leu) c.2893T>C (p.Phe965Leu) c.2857T>C (p.Phe953Leu) | gnomAD v4 |
| 19 | g.7128901A>T | CA304876031 | INSR | c.2896T>A (p.Phe966Ile) c.2860T>A (p.Phe954Ile) c.2971T>A (p.Phe991Ile) c.2935T>A (p.Phe979Ile) c.2893T>A (p.Phe965Ile) c.2857T>A (p.Phe953Ile) | dbSNP |
| 19 | g.7128902G>A | CA505217393 | INSR | c.2895C>T (p.Val965=) c.2859C>T (p.Val953=) c.2970C>T (p.Val990=) c.2934C>T (p.Val978=) c.2892C>T (p.Val964=) c.2856C>T (p.Val952=) | |
| 19 | g.7128902G>C | CA505217394 | INSR | c.2895C>G (p.Val965=) c.2859C>G (p.Val953=) c.2970C>G (p.Val990=) c.2934C>G (p.Val978=) c.2892C>G (p.Val964=) c.2856C>G (p.Val952=) | |
| 19 | g.7128902G>T | CA505217395 | INSR | c.2895C>A (p.Val965=) c.2859C>A (p.Val953=) c.2970C>A (p.Val990=) c.2934C>A (p.Val978=) c.2892C>A (p.Val964=) c.2856C>A (p.Val952=) | COSMIC COSMIC |
| 19 | g.7128903A>C | CA403671770 | INSR | c.2894T>G (p.Val965Gly) c.2858T>G (p.Val953Gly) c.2969T>G (p.Val990Gly) c.2933T>G (p.Val978Gly) c.2891T>G (p.Val964Gly) c.2855T>G (p.Val952Gly) | |
| 19 | g.7128903A>G | CA403671771 | INSR | c.2894T>C (p.Val965Ala) c.2858T>C (p.Val953Ala) c.2969T>C (p.Val990Ala) c.2933T>C (p.Val978Ala) c.2891T>C (p.Val964Ala) c.2855T>C (p.Val952Ala) | |
| 19 | g.7128903A>T | CA403671772 | INSR | c.2894T>A (p.Val965Asp) c.2858T>A (p.Val953Asp) c.2969T>A (p.Val990Asp) c.2933T>A (p.Val978Asp) c.2891T>A (p.Val964Asp) c.2855T>A (p.Val952Asp) | |
| 19 | g.7128904C>A | CA403671775 | INSR | c.2893G>T (p.Val965Phe) c.2857G>T (p.Val953Phe) c.2968G>T (p.Val990Phe) c.2932G>T (p.Val978Phe) c.2890G>T (p.Val964Phe) c.2854G>T (p.Val952Phe) | |
| 19 | g.7128904C= | CA2320769470 | INSR | c.2893G= (p.Val965=) c.2857G= (p.Val953=) c.2968G= (p.Val990=) c.2932G= (p.Val978=) c.2890G= (p.Val964=) c.2854G= (p.Val952=) | |
| 19 | g.7128904C>G | CA403671774 | INSR | c.2893G>C (p.Val965Leu) c.2857G>C (p.Val953Leu) c.2968G>C (p.Val990Leu) c.2932G>C (p.Val978Leu) c.2890G>C (p.Val964Leu) c.2854G>C (p.Val952Leu) | |
| 19 | g.7128904C>T | CA403671773 | INSR | c.2893G>A (p.Val965Ile) c.2857G>A (p.Val953Ile) c.2968G>A (p.Val990Ile) c.2932G>A (p.Val978Ile) c.2890G>A (p.Val964Ile) c.2854G>A (p.Val952Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.7128905A>C | CA403671776 | INSR | c.2892T>G (p.Phe964Leu) c.2856T>G (p.Phe952Leu) c.2967T>G (p.Phe989Leu) c.2931T>G (p.Phe977Leu) c.2889T>G (p.Phe963Leu) c.2853T>G (p.Phe951Leu) | |
| 19 | g.7128905A>G | CA505217397 | INSR | c.2892T>C (p.Phe964=) c.2856T>C (p.Phe952=) c.2967T>C (p.Phe989=) c.2931T>C (p.Phe977=) c.2889T>C (p.Phe963=) c.2853T>C (p.Phe951=) | |
| 19 | g.7128905A>T | CA403671777 | INSR | c.2892T>A (p.Phe964Leu) c.2856T>A (p.Phe952Leu) c.2967T>A (p.Phe989Leu) c.2931T>A (p.Phe977Leu) c.2889T>A (p.Phe963Leu) c.2853T>A (p.Phe951Leu) | |
| 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=) |