Canonical Allele Identifier: CA463860129
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2879399
ClinVar RCV Id: RCV003710699
dbSNP Id: rs1818183940
MyVariant Identifiers: chr9:g.12702332A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12702332A>G , CM000671.2:g.12702332A>G GRCh38
NC_000009.11:g.12702332A>G , CM000671.1:g.12702332A>G GRCh37
NC_000009.10:g.12692332A>G NCBI36
NG_011705.1:g.13947A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.975A>G (TYRP1) MANE Select ENSP00000373570.4:p.Gln325=
ENST00000381136.2:c.105A>G (TYRP1) ENSP00000370528.2:p.Gln35=
ENST00000381142.3:n.212A>G (TYRP1)
ENST00000388918.9:c.975A>G (TYRP1) ENSP00000373570.4:p.Gln325=
ENST00000470909.1:n.233A>G (TYRP1)
NM_000550.2:c.975A>G (TYRP1) NP_000541.1:p.Gln325=
NR_125775.1:n.317-1706T>C (LURAP1L-AS1)
XR_001746372.2:n.959A>G (TYRP1)
NM_000550.3:c.975A>G (TYRP1) MANE Select NP_000541.1:p.Gln325=