Canonical Allele Identifier: CA2579301248
Gene: TYRP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12695439A>G , CM000671.2:g.12695439A>G GRCh38
NC_000009.11:g.12695439A>G , CM000671.1:g.12695439A>G GRCh37
NC_000009.10:g.12685439A>G NCBI36
NG_011705.1:g.7054A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.386-76A>G MANE Select ENSP00000373570.4:n.386-76A>G
ENST00000388918.9:c.386-76A>G ENSP00000373570.4:n.386-76A>G
NM_000550.2:c.386-76A>G NP_000541.1:n.386-76A>G
XR_001746372.2:n.575-76A>G
NM_000550.3:c.386-76A>G MANE Select NP_000541.1:n.386-76A>G