Canonical Allele Identifier: CA372936990
Gene: TYRP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695532G>T , CM000671.2:g.12695532G>T GRCh38
NC_000009.11:g.12695532G>T , CM000671.1:g.12695532G>T GRCh37
NC_000009.10:g.12685532G>T NCBI36
NG_011705.1:g.7147G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.403G>T MANE Select ENSP00000373570.4:p.Asp135Tyr
ENST00000388918.9:c.403G>T ENSP00000373570.4:p.Asp135Tyr
NM_000550.2:c.403G>T NP_000541.1:p.Asp135Tyr
XR_001746372.2:n.592G>T
NM_000550.3:c.403G>T MANE Select NP_000541.1:p.Asp135Tyr