Canonical Allele Identifier: CA463860119
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1563855000
MyVariant Identifiers: chr9:g.12702317C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12702317C>G , CM000671.2:g.12702317C>G GRCh38
NC_000009.11:g.12702317C>G , CM000671.1:g.12702317C>G GRCh37
NC_000009.10:g.12692317C>G NCBI36
NG_011705.1:g.13932C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.960C>G (TYRP1) MANE Select ENSP00000373570.4:p.Ala320=
ENST00000381136.2:c.90C>G (TYRP1) ENSP00000370528.2:p.Ala30=
ENST00000381142.3:n.197C>G (TYRP1)
ENST00000388918.9:c.960C>G (TYRP1) ENSP00000373570.4:p.Ala320=
ENST00000470909.1:n.218C>G (TYRP1)
NM_000550.2:c.960C>G (TYRP1) NP_000541.1:p.Ala320=
NR_125775.1:n.317-1691G>C (LURAP1L-AS1)
XR_001746372.2:n.944C>G (TYRP1)
NM_000550.3:c.960C>G (TYRP1) MANE Select NP_000541.1:p.Ala320=