Canonical Allele Identifier: CA2689402647
Gene: TYRP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695455del , CM000671.2:g.12695455del GRCh38
NC_000009.11:g.12695455del , CM000671.1:g.12695455del GRCh37
NC_000009.10:g.12685455del NCBI36
NG_011705.1:g.7070del

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.386-60del MANE Select ENSP00000373570.4:n.386-60del
ENST00000388918.9:c.386-60del ENSP00000373570.4:n.386-60del
NM_000550.2:c.386-60del NP_000541.1:n.386-60del
XR_001746372.2:n.575-60del
NM_000550.3:c.386-60del MANE Select NP_000541.1:n.386-60del