Canonical Allele Identifier: CA463860284
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2873690
ClinVar RCV Id: RCV003712037
dbSNP Id: rs1334028491
gnomAD v2: 9-12704590-A-G
gnomAD v3: 9-12704590-A-G
gnomAD v4: 9-12704590-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12704590A>G , CM000671.2:g.12704590A>G GRCh38
NC_000009.11:g.12704590A>G , CM000671.1:g.12704590A>G GRCh37
NC_000009.10:g.12694590A>G NCBI36
NG_011705.1:g.16205A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.1146A>G (TYRP1) MANE Select ENSP00000373570.4:p.Leu382=
ENST00000381136.2:c.276A>G (TYRP1) ENSP00000370528.2:p.Leu92=
ENST00000381142.3:n.383A>G (TYRP1)
ENST00000388918.9:c.1146A>G (TYRP1) ENSP00000373570.4:p.Leu382=
NM_000550.2:c.1146A>G (TYRP1) NP_000541.1:p.Leu382=
NR_125775.1:n.317-3964T>C (LURAP1L-AS1)
XR_001746372.2:n.1130A>G (TYRP1)
NM_000550.3:c.1146A>G (TYRP1) MANE Select NP_000541.1:p.Leu382=