Canonical Allele Identifier: CA189313872
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3010127
ClinVar RCV Id: RCV003867302
dbSNP Id: rs541742268
gnomAD v3: 9-12704542-G-A
gnomAD v4: 9-12704542-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12704542G>A , CM000671.2:g.12704542G>A GRCh38
NC_000009.11:g.12704542G>A , CM000671.1:g.12704542G>A GRCh37
NC_000009.10:g.12694542G>A NCBI36
NG_011705.1:g.16157G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.1098G>A (TYRP1) MANE Select ENSP00000373570.4:p.Thr366=
ENST00000381136.2:c.228G>A (TYRP1) ENSP00000370528.2:p.Thr76=
ENST00000381142.3:n.335G>A (TYRP1)
ENST00000388918.9:c.1098G>A (TYRP1) ENSP00000373570.4:p.Thr366=
NM_000550.2:c.1098G>A (TYRP1) NP_000541.1:p.Thr366=
NR_125775.1:n.317-3916C>T (LURAP1L-AS1)
XR_001746372.2:n.1082G>A (TYRP1)
NM_000550.3:c.1098G>A (TYRP1) MANE Select NP_000541.1:p.Thr366=