Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48487200T>A , CM000677.2:g.48487200T>A | GRCh38 |
| NC_000015.9:g.48779397T>A , CM000677.1:g.48779397T>A | GRCh37 |
| NC_000015.8:g.46566689T>A | NCBI36 |
| NG_008805.2:g.163589A>T , LRG_778:g.163589A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000138.5:c.3464A>T MANE Select | NP_000129.3:p.Asp1155Val |
| ENST00000316623.10:c.3464A>T MANE Select | ENSP00000325527.5:p.Asp1155Val |
| NM_000138.4:c.3464A>T , LRG_778t1:c.3464A>T | NP_000129.3:p.Asp1155Val |
| ENST00000316623.9:c.3464A>T | ENSP00000325527.5:p.Asp1155Val |
| ENST00000537463.6:c.637-12550A>T | ENSP00000440294.2:n.637-12550A>T |
| ENST00000559133.6:c.3464A>T | ENSP00000453958.2:p.Asp1155Val |
| ENST00000674301.2:c.3464A>T | ENSP00000501333.2:p.Asp1155Val |
| ENST00000684448.1:n.2138A>T |