Canonical Allele Identifier: CA2782943161
Gene: TYRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695446_12695447del , CM000671.2:g.12695446_12695447del GRCh38
NC_000009.11:g.12695446_12695447del , CM000671.1:g.12695446_12695447del GRCh37
NC_000009.10:g.12685446_12685447del NCBI36
NG_011705.1:g.7061_7062del

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.386-69_386-68del MANE Select ENSP00000373570.4:n.386-69_386-68del
ENST00000388918.9:c.386-69_386-68del ENSP00000373570.4:n.386-69_386-68del
NM_000550.2:c.386-69_386-68del NP_000541.1:n.386-69_386-68del
XR_001746372.2:n.575-69_575-68del
NM_000550.3:c.386-69_386-68del MANE Select NP_000541.1:n.386-69_386-68del