Canonical Allele Identifier: CA372937268
Gene: TYRP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695630A>C , CM000671.2:g.12695630A>C GRCh38
NC_000009.11:g.12695630A>C , CM000671.1:g.12695630A>C GRCh37
NC_000009.10:g.12685630A>C NCBI36
NG_011705.1:g.7245A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.501A>C MANE Select ENSP00000373570.4:p.Glu167Asp
ENST00000388918.9:c.501A>C ENSP00000373570.4:p.Glu167Asp
NM_000550.2:c.501A>C NP_000541.1:p.Glu167Asp
XR_001746372.2:n.690A>C
NM_000550.3:c.501A>C MANE Select NP_000541.1:p.Glu167Asp