Canonical Allele Identifier: CA372937305
Gene: TYRP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695638T>C , CM000671.2:g.12695638T>C GRCh38
NC_000009.11:g.12695638T>C , CM000671.1:g.12695638T>C GRCh37
NC_000009.10:g.12685638T>C NCBI36
NG_011705.1:g.7253T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.509T>C MANE Select ENSP00000373570.4:p.Leu170Pro
ENST00000388918.9:c.509T>C ENSP00000373570.4:p.Leu170Pro
NM_000550.2:c.509T>C NP_000541.1:p.Leu170Pro
XR_001746372.2:n.698T>C
NM_000550.3:c.509T>C MANE Select NP_000541.1:p.Leu170Pro