Canonical Allele Identifier: CA372936999
Gene: TYRP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695536T>A , CM000671.2:g.12695536T>A GRCh38
NC_000009.11:g.12695536T>A , CM000671.1:g.12695536T>A GRCh37
NC_000009.10:g.12685536T>A NCBI36
NG_011705.1:g.7151T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.407T>A MANE Select ENSP00000373570.4:p.Leu136Ter
ENST00000388918.9:c.407T>A ENSP00000373570.4:p.Leu136Ter
NM_000550.2:c.407T>A NP_000541.1:p.Leu136Ter
XR_001746372.2:n.596T>A
NM_000550.3:c.407T>A MANE Select NP_000541.1:p.Leu136Ter