Canonical Allele Identifier: CA189313985
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2903561
ClinVar RCV Id: RCV003726783
dbSNP Id: rs142112882
gnomAD v2: 9-12704584-T-A
gnomAD v3: 9-12704584-T-A
gnomAD v4: 9-12704584-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12704584T>A , CM000671.2:g.12704584T>A GRCh38
NC_000009.11:g.12704584T>A , CM000671.1:g.12704584T>A GRCh37
NC_000009.10:g.12694584T>A NCBI36
NG_011705.1:g.16199T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.1140T>A (TYRP1) MANE Select ENSP00000373570.4:p.Ala380=
ENST00000381136.2:c.270T>A (TYRP1) ENSP00000370528.2:p.Ala90=
ENST00000381142.3:n.377T>A (TYRP1)
ENST00000388918.9:c.1140T>A (TYRP1) ENSP00000373570.4:p.Ala380=
NM_000550.2:c.1140T>A (TYRP1) NP_000541.1:p.Ala380=
NR_125775.1:n.317-3958A>T (LURAP1L-AS1)
XR_001746372.2:n.1124T>A (TYRP1)
NM_000550.3:c.1140T>A (TYRP1) MANE Select NP_000541.1:p.Ala380=