Canonical Allele Identifier: CA1834018135
Gene: TYRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695442A= , CM000671.2:g.12695442A= GRCh38
NC_000009.11:g.12695442A= , CM000671.1:g.12695442A= GRCh37
NC_000009.10:g.12685442A= NCBI36
NG_011705.1:g.7057A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.386-73A= MANE Select ENSP00000373570.4:n.386-73A=
ENST00000388918.9:c.386-73A= ENSP00000373570.4:n.386-73A=
NM_000550.2:c.386-73A= NP_000541.1:n.386-73A=
XR_001746372.2:n.575-73A=
NM_000550.3:c.386-73A= MANE Select NP_000541.1:n.386-73A=