Canonical Allele Identifier: CA463860341
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2118259182
gnomAD v3: 9-12704647-C-T
gnomAD v4: 9-12704647-C-T
MyVariant Identifiers: chr9:g.12704647C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12704647C>T , CM000671.2:g.12704647C>T GRCh38
NC_000009.11:g.12704647C>T , CM000671.1:g.12704647C>T GRCh37
NC_000009.10:g.12694647C>T NCBI36
NG_011705.1:g.16262C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000388918.10:c.1203C>T (TYRP1) MANE Select ENSP00000373570.4:p.Val401=
ENST00000381136.2:c.333C>T (TYRP1) ENSP00000370528.2:p.Val111=
ENST00000381142.3:n.440C>T (TYRP1)
ENST00000388918.9:c.1203C>T (TYRP1) ENSP00000373570.4:p.Val401=
NM_000550.2:c.1203C>T (TYRP1) NP_000541.1:p.Val401=
NR_125775.1:n.317-4021G>A (LURAP1L-AS1)
XR_001746372.2:n.1187C>T (TYRP1)
NM_000550.3:c.1203C>T (TYRP1) MANE Select NP_000541.1:p.Val401=