Canonical Allele Identifier: CA372936984
Gene: TYRP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695527T>G , CM000671.2:g.12695527T>G GRCh38
NC_000009.11:g.12695527T>G , CM000671.1:g.12695527T>G GRCh37
NC_000009.10:g.12685527T>G NCBI36
NG_011705.1:g.7142T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.398T>G MANE Select ENSP00000373570.4:p.Leu133Arg
ENST00000388918.9:c.398T>G ENSP00000373570.4:p.Leu133Arg
NM_000550.2:c.398T>G NP_000541.1:p.Leu133Arg
XR_001746372.2:n.587T>G
NM_000550.3:c.398T>G MANE Select NP_000541.1:p.Leu133Arg