UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.37050614T= , CM000665.2:g.37050614T= | GRCh38 |
| NC_000003.11:g.37092105T= , CM000665.1:g.37092105T= | GRCh37 |
| NC_000003.10:g.37067109T= | NCBI36 |
| NG_007109.2:g.62265T= , LRG_216:g.62265T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000413740.2:c.1796T= | ENSP00000416476.2:p.Leu599= | |
| ENST00000429117.6:c.1938T= | ENSP00000407019.2:p.Ala646= | |
| ENST00000456676.7:c.2025T= | ENSP00000416687.3:p.Ala675= | |
| ENST00000492474.6:c.1509T= | ENSP00000518393.1:p.Ala503= | |
| ENST00000616768.6:c.2139T= | ENSP00000480669.3:p.Ala713= | |
| ENST00000673673.2:c.2067T= | ENSP00000500979.2:p.Ala689= | |
| ENST00000231790.8:c.2232T= MANE Select | ENSP00000231790.3:p.Ala744= | |
| ENST00000413212.2:c.*1150T= | ENSP00000400844.2:n.*1150T= | |
| ENST00000432299.6:c.*2064T= | ENSP00000416783.1:n.*2064T= | |
| ENST00000447829.6:c.*1343T= | ENSP00000399329.2:n.*1343T= | |
| ENST00000539477.6:c.1509T= | ENSP00000443665.1:p.Ala503= | |
| ENST00000616768.5:c.1176T= | ENSP00000480669.2:p.Ala392= | |
| ENST00000673673.1:c.2020T= | ||
| ENST00000673741.1:n.1266T= | ||
| ENST00000673889.1:n.1614T= | ||
| ENST00000673897.1:c.*2024T= | ENSP00000501109.1:n.*2024T= | |
| ENST00000673899.1:c.1500T= | ENSP00000501030.1:p.Ala500= | |
| ENST00000673947.1:c.*2372T= | ENSP00000501304.1:n.*2372T= | |
| ENST00000673972.1:c.*2110T= | ENSP00000501281.1:n.*2110T= | |
| ENST00000674019.1:c.1509T= | ENSP00000501081.1:p.Ala503= | |
| ENST00000674111.1:c.*461T= | ENSP00000501162.1:n.*461T= | |
| ENST00000674125.1:n.943T= | ||
| ENST00000231790.6:c.2232T= | ENSP00000231790.2:p.Ala744= | |
| ENST00000435176.5:c.1938T= | ENSP00000402564.1:p.Ala646= | |
| ENST00000455445.6:c.1509T= | ENSP00000398272.2:p.Ala503= | |
| ENST00000456676.6:c.2000T= | ||
| ENST00000458205.6:c.1509T= | ENSP00000402667.2:p.Ala503= | |
| ENST00000536378.5:c.1509T= | ENSP00000444286.2:p.Ala503= | |
| ENST00000539477.5:c.1509T= | ENSP00000443665.1:p.Ala503= | |
| NM_000249.3:c.2232T= , LRG_216t1:c.2232T= | NP_000240.1:p.Ala744= | |
| NM_001167617.1:c.1938T= | NP_001161089.1:p.Ala646= | |
| NM_001167618.1:c.1509T= | NP_001161090.1:p.Ala503= | |
| NM_001167619.1:c.1509T= | NP_001161091.1:p.Ala503= | |
| NM_001258271.1:c.2025T= | NP_001245200.1:p.Ala675= | |
| NM_001258273.1:c.1509T= | NP_001245202.1:p.Ala503= | |
| NM_001258274.1:c.1509T= | NP_001245203.1:p.Ala503= | |
| XM_005265161.1:c.2025T= | XP_005265218.1:p.Ala675= | |
| XM_005265163.1:c.1509T= | XP_005265220.1:p.Ala503= | |
| XM_005265164.1:c.1509T= | XP_005265221.1:p.Ala503= | |
| XM_005265166.1:c.1209T= | XP_005265223.1:p.Ala403= | |
| XM_011533727.1:c.1158T= | XP_011532029.1:p.Ala386= | |
| NM_001167617.2:c.1938T= | NP_001161089.1:p.Ala646= | |
| NM_001167618.2:c.1509T= | NP_001161090.1:p.Ala503= | |
| NM_001167619.2:c.1509T= | NP_001161091.1:p.Ala503= | |
| NM_001258274.2:c.1509T= | NP_001245203.1:p.Ala503= | |
| NM_001354615.1:c.1509T= | NP_001341544.1:p.Ala503= | |
| NM_001354616.1:c.1509T= | NP_001341545.1:p.Ala503= | |
| NM_001354617.1:c.1509T= | NP_001341546.1:p.Ala503= | |
| NM_001354618.1:c.1509T= | NP_001341547.1:p.Ala503= | |
| NM_001354619.1:c.1509T= | NP_001341548.1:p.Ala503= | |
| NM_001354620.1:c.1938T= | NP_001341549.1:p.Ala646= | |
| NM_001354621.1:c.1209T= | NP_001341550.1:p.Ala403= | |
| NM_001354622.1:c.1209T= | NP_001341551.1:p.Ala403= | |
| NM_001354623.1:c.1209T= | NP_001341552.1:p.Ala403= | |
| NM_001354624.1:c.1158T= | NP_001341553.1:p.Ala386= | |
| NM_001354625.1:c.1158T= | NP_001341554.1:p.Ala386= | |
| NM_001354626.1:c.1158T= | NP_001341555.1:p.Ala386= | |
| NM_001354627.1:c.1158T= | NP_001341556.1:p.Ala386= | |
| NM_001354628.1:c.2139T= | NP_001341557.1:p.Ala713= | |
| NM_001354629.1:c.2133T= | NP_001341558.1:p.Ala711= | |
| NM_001354630.1:c.2067T= | NP_001341559.1:p.Ala689= | |
| XM_005265161.2:c.2025T= | XP_005265218.1:p.Ala675= | |
| XM_017006450.2:c.1209T= | XP_016861939.1:p.Ala403= | |
| NM_000249.4:c.2232T= MANE Select | NP_000240.1:p.Ala744= | |
| NM_001167617.3:c.1938T= | NP_001161089.1:p.Ala646= | |
| NM_001167618.3:c.1509T= | NP_001161090.1:p.Ala503= | |
| NM_001167619.3:c.1509T= | NP_001161091.1:p.Ala503= | |
| NM_001258271.2:c.2025T= | NP_001245200.1:p.Ala675= | |
| NM_001258273.2:c.1509T= | NP_001245202.1:p.Ala503= | |
| NM_001258274.3:c.1509T= | NP_001245203.1:p.Ala503= | |
| NM_001354615.2:c.1509T= | NP_001341544.1:p.Ala503= | |
| NM_001354616.2:c.1509T= | NP_001341545.1:p.Ala503= | |
| NM_001354617.2:c.1509T= | NP_001341546.1:p.Ala503= | |
| NM_001354618.2:c.1509T= | NP_001341547.1:p.Ala503= | |
| NM_001354619.2:c.1509T= | NP_001341548.1:p.Ala503= | |
| NM_001354620.2:c.1938T= | NP_001341549.1:p.Ala646= | |
| NM_001354621.2:c.1209T= | NP_001341550.1:p.Ala403= | |
| NM_001354622.2:c.1209T= | NP_001341551.1:p.Ala403= | |
| NM_001354623.2:c.1209T= | NP_001341552.1:p.Ala403= | |
| NM_001354624.2:c.1158T= | NP_001341553.1:p.Ala386= | |
| NM_001354625.2:c.1158T= | NP_001341554.1:p.Ala386= | |
| NM_001354626.2:c.1158T= | NP_001341555.1:p.Ala386= | |
| NM_001354627.2:c.1158T= | NP_001341556.1:p.Ala386= | |
| NM_001354628.2:c.2139T= | NP_001341557.1:p.Ala713= | |
| NM_001354629.2:c.2133T= | NP_001341558.1:p.Ala711= | |
| NM_001354630.2:c.2067T= | NP_001341559.1:p.Ala689= |