Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153691338C>A , CM000685.2:g.153691338C>A | GRCh38 |
| NC_000023.10:g.152956793C>A , CM000685.1:g.152956793C>A | GRCh37 |
| NC_000023.9:g.152609987C>A | NCBI36 |
| NG_012016.1:g.8042C>A | |
| NG_012016.2:g.8042C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005629.4:c.429C>A MANE Select | NP_005620.1:p.Tyr143Ter |
| ENST00000253122.10:c.429C>A MANE Select | ENSP00000253122.5:p.Tyr143Ter |
| NM_001142805.1:c.429C>A | NP_001136277.1:p.Tyr143Ter |
| NM_001142805.2:c.429C>A | NP_001136277.1:p.Tyr143Ter |
| NM_001142806.1:c.84C>A | NP_001136278.1:p.Tyr28Ter |
| NM_005629.3:c.429C>A | NP_005620.1:p.Tyr143Ter |
| ENST00000253122.9:c.429C>A | ENSP00000253122.5:p.Tyr143Ter |
| ENST00000430077.6:c.84C>A | ENSP00000403041.2:p.Tyr28Ter |
| ENST00000466243.1:n.221C>A | |
| ENST00000675713.1:n.183C>A |