Canonical Allele Identifier: CA372936992
Gene: TYRP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695533A>G , CM000671.2:g.12695533A>G GRCh38
NC_000009.11:g.12695533A>G , CM000671.1:g.12695533A>G GRCh37
NC_000009.10:g.12685533A>G NCBI36
NG_011705.1:g.7148A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.404A>G MANE Select ENSP00000373570.4:p.Asp135Gly
ENST00000388918.9:c.404A>G ENSP00000373570.4:p.Asp135Gly
NM_000550.2:c.404A>G NP_000541.1:p.Asp135Gly
XR_001746372.2:n.593A>G
NM_000550.3:c.404A>G MANE Select NP_000541.1:p.Asp135Gly