Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.81363898T>A , CM000678.2:g.81363898T>A | GRCh38 |
| NC_000016.9:g.81397503T>A , CM000678.1:g.81397503T>A | GRCh37 |
| NC_000016.8:g.79955004T>A | NCBI36 |
| NG_009007.1:g.53933T>A , LRG_242:g.53933T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022041.4:c.1191T>A MANE Select | NP_071324.1:p.Tyr397Ter |
| ENST00000648994.2:c.1191T>A MANE Select | ENSP00000497351.1:p.Tyr397Ter |
| NM_001377486.1:c.552T>A | NP_001364415.1:p.Tyr184Ter |
| NM_022041.3:c.1191T>A , LRG_242t1:c.1191T>A | NP_071324.1:p.Tyr397Ter |
| ENST00000568107.2:c.1191T>A | ENSP00000476795.1:p.Tyr397Ter |
| ENST00000648349.2:c.*899T>A | ENSP00000498114.1:n.*899T>A |
| ENST00000650388.1:c.725T>A | ENSP00000498081.1:n.725T>A |
| XM_017023734.1:c.552T>A | XP_016879223.1:p.Tyr184Ter |