Linked Data
MyVariant Identifiers:
chr1:g.120295910A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119753287A>T , CM000663.2:g.119753287A>T | GRCh38 |
| NC_000001.10:g.120295910A>T , CM000663.1:g.120295910A>T | GRCh37 |
| NC_000001.9:g.120097433A>T | NCBI36 |
| NG_013348.1:g.20646T>A , LRG_447:g.20646T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369406.8:c.1287T>A MANE Select | ENSP00000358414.3:p.Ala429= | |
| ENST00000369406.7:c.1287T>A | ENSP00000358414.3:p.Ala429= | |
| ENST00000544913.2:c.1161T>A | ENSP00000439495.2:p.Ala387= | |
| NM_001166107.1:c.1161T>A , LRG_447t2:c.1161T>A | NP_001159579.1:p.Ala387= | |
| NM_005518.3:c.1287T>A , LRG_447t1:c.1287T>A | NP_005509.1:p.Ala429= | |
| XM_011541313.1:c.1122T>A | XP_011539615.1:p.Ala374= | |
| XM_011541313.2:c.1122T>A | XP_011539615.1:p.Ala374= | |
| NM_005518.4:c.1287T>A MANE Select | NP_005509.1:p.Ala429= |