Canonical Allele Identifier: CA372937027
Gene: TYRP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695548A>C , CM000671.2:g.12695548A>C GRCh38
NC_000009.11:g.12695548A>C , CM000671.1:g.12695548A>C GRCh37
NC_000009.10:g.12685548A>C NCBI36
NG_011705.1:g.7163A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.419A>C MANE Select ENSP00000373570.4:p.Glu140Ala
ENST00000388918.9:c.419A>C ENSP00000373570.4:p.Glu140Ala
NM_000550.2:c.419A>C NP_000541.1:p.Glu140Ala
XR_001746372.2:n.608A>C
NM_000550.3:c.419A>C MANE Select NP_000541.1:p.Glu140Ala