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.189890825_189890826insA , CM000665.2:g.189890825_189890826insA | GRCh38 |
| NC_000003.11:g.189608614_189608615insA , CM000665.1:g.189608614_189608615insA | GRCh37 |
| NC_000003.10:g.191091308_191091309insA | NCBI36 |
| NG_007550.1:g.264399_264400insA | |
| NG_007550.2:g.264399_264400insA | |
| NG_007550.3:g.299080_299081insA |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264731.8:c.1689_1690insA MANE Select | ENSP00000264731.3:p.Tyr564IlefsTer14 | |
| ENST00000354600.10:c.1407_1408insA MANE Plus Clinical | ENSP00000346614.5:p.Tyr470IlefsTer14 | |
| ENST00000264731.7:c.1689_1690insA | ENSP00000264731.3:p.Tyr564IlefsTer14 | |
| ENST00000320472.9:c.1508-3381_1508-3380insA | ENSP00000317510.5:n.1508-3381_1508-3380in... | |
| ENST00000354600.9:c.1407_1408insA | ENSP00000346614.5:p.Tyr470IlefsTer14 | |
| ENST00000392460.7:c.1652+1341_1652+1342insA | ENSP00000376253.3:n.1652+1341_1652+1342in... | |
| ENST00000392461.7:c.1226-3381_1226-3380insA | ENSP00000376254.3:n.1226-3381_1226-3380in... | |
| ENST00000392463.6:c.1370+1341_1370+1342insA | ENSP00000376256.2:n.1370+1341_1370+1342in... | |
| ENST00000440651.6:c.1677_1678insA | ENSP00000394337.2:p.Tyr560IlefsTer14 | |
| ENST00000449992.5:c.1152_1153insA | ENSP00000387839.1:p.Tyr385IlefsTer14 | |
| ENST00000456148.1:c.1395_1396insA | ENSP00000389485.1:p.Tyr466IlefsTer14 | |
| NM_001114978.1:c.1652+1341_1652+1342insA | NP_001108450.1:n.1652+1341_1652+1342insA | |
| NM_001114980.1:c.1407_1408insA | NP_001108452.1:p.Tyr470IlefsTer14 | |
| NM_001114981.1:c.1370+1341_1370+1342insA | NP_001108453.1:n.1370+1341_1370+1342insA | |
| NM_003722.4:c.1689_1690insA | NP_003713.3:p.Tyr564IlefsTer14 | |
| XM_005247843.2:c.1677_1678insA | XP_005247900.1:p.Tyr560IlefsTer14 | |
| XM_005247844.3:c.1638_1639insA | XP_005247901.1:p.Tyr547IlefsTer14 | |
| XM_011513251.1:c.1686_1687insA | XP_011511553.1:p.Tyr563IlefsTer14 | |
| XM_011513252.1:c.1683_1684insA | XP_011511554.1:p.Tyr562IlefsTer14 | |
| XM_011513253.1:c.1650_1651insA | XP_011511555.1:p.Tyr551IlefsTer14 | |
| NM_001329144.1:c.1508-3381_1508-3380insA | NP_001316073.1:n.1508-3381_1508-3380insA | |
| NM_001329145.1:c.1226-3381_1226-3380insA | NP_001316074.1:n.1226-3381_1226-3380insA | |
| NM_001329146.1:c.1152_1153insA | NP_001316075.1:p.Tyr385IlefsTer14 | |
| NM_001329148.1:c.1677_1678insA | NP_001316077.1:p.Tyr560IlefsTer14 | |
| NM_001329149.1:c.1214-3381_1214-3380insA | NP_001316078.1:n.1214-3381_1214-3380insA | |
| NM_001329150.1:c.959-3381_959-3380insA | NP_001316079.1:n.959-3381_959-3380insA | |
| NM_001329964.1:c.1683_1684insA | NP_001316893.1:p.Tyr562IlefsTer14 | |
| NM_003722.5:c.1689_1690insA MANE Select | NP_003713.3:p.Tyr564IlefsTer14 | |
| NM_001114978.2:c.1652+1341_1652+1342insA | NP_001108450.1:n.1652+1341_1652+1342insA | |
| NM_001114980.2:c.1407_1408insA MANE Plus Clinical | NP_001108452.1:p.Tyr470IlefsTer14 | |
| NM_001114981.2:c.1370+1341_1370+1342insA | NP_001108453.1:n.1370+1341_1370+1342insA | |
| NM_001329144.2:c.1508-3381_1508-3380insA | NP_001316073.1:n.1508-3381_1508-3380insA | |
| NM_001329145.2:c.1226-3381_1226-3380insA | NP_001316074.1:n.1226-3381_1226-3380insA | |
| NM_001329146.2:c.1152_1153insA | NP_001316075.1:p.Tyr385IlefsTer14 | |
| NM_001329148.2:c.1677_1678insA | NP_001316077.1:p.Tyr560IlefsTer14 | |
| NM_001329149.2:c.1214-3381_1214-3380insA | NP_001316078.1:n.1214-3381_1214-3380insA | |
| NM_001329150.2:c.959-3381_959-3380insA | NP_001316079.1:n.959-3381_959-3380insA | |
| NM_001329964.2:c.1683_1684insA | NP_001316893.1:p.Tyr562IlefsTer14 |