Canonical Allele Identifier: CA209368
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 212526
dbSNP Id: rs184910238
gnomAD v2: 9-12704582-G-T
gnomAD v3: 9-12704582-G-T
gnomAD v4: 9-12704582-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12704582G>T , CM000671.2:g.12704582G>T GRCh38
NC_000009.11:g.12704582G>T , CM000671.1:g.12704582G>T GRCh37
NC_000009.10:g.12694582G>T NCBI36
NG_011705.1:g.16197G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.1138G>T (TYRP1) MANE Select ENSP00000373570.4:p.Ala380Ser
ENST00000381136.2:c.268G>T (TYRP1) ENSP00000370528.2:p.Ala90Ser
ENST00000381142.3:n.375G>T (TYRP1)
ENST00000388918.9:c.1138G>T (TYRP1) ENSP00000373570.4:p.Ala380Ser
NM_000550.2:c.1138G>T (TYRP1) NP_000541.1:p.Ala380Ser
NR_125775.1:n.317-3956C>A (LURAP1L-AS1)
XR_001746372.2:n.1122G>T (TYRP1)
NM_000550.3:c.1138G>T (TYRP1) MANE Select NP_000541.1:p.Ala380Ser