Canonical Allele Identifier: CA463860368
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1376871155
gnomAD v2: 9-12704671-A-G
gnomAD v4: 9-12704671-A-G
MyVariant Identifiers: chr9:g.12704671A>G (hg19) chr9:g.12704671A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12704671A>G , CM000671.2:g.12704671A>G GRCh38
NC_000009.11:g.12704671A>G , CM000671.1:g.12704671A>G GRCh37
NC_000009.10:g.12694671A>G NCBI36
NG_011705.1:g.16286A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.1227A>G (TYRP1) MANE Select ENSP00000373570.4:p.Ala409=
ENST00000381136.2:c.357A>G (TYRP1) ENSP00000370528.2:p.Ala119=
ENST00000381142.3:n.464A>G (TYRP1)
ENST00000388918.9:c.1227A>G (TYRP1) ENSP00000373570.4:p.Ala409=
NM_000550.2:c.1227A>G (TYRP1) NP_000541.1:p.Ala409=
NR_125775.1:n.317-4045T>C (LURAP1L-AS1)
XR_001746372.2:n.1211A>G (TYRP1)
NM_000550.3:c.1227A>G (TYRP1) MANE Select NP_000541.1:p.Ala409=
Search 100 bp 5'
Search 100 bp 3'