Canonical Allele Identifier: CA463860547
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.12708130A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12708130A>G , CM000671.2:g.12708130A>G GRCh38
NC_000009.11:g.12708130A>G , CM000671.1:g.12708130A>G GRCh37
NC_000009.10:g.12698130A>G NCBI36
NG_011705.1:g.19745A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.1395A>G (TYRP1) MANE Select ENSP00000373570.4:p.Glu465=
ENST00000381136.2:c.525A>G (TYRP1) ENSP00000370528.2:p.Glu175=
ENST00000381142.3:n.499-847A>G (TYRP1)
ENST00000388918.9:c.1395A>G (TYRP1) ENSP00000373570.4:p.Glu465=
ENST00000473504.1:n.460A>G (TYRP1)
NM_000550.2:c.1395A>G (TYRP1) NP_000541.1:p.Glu465=
NR_125775.1:n.317-7504T>C (LURAP1L-AS1)
XR_001746372.2:n.1379A>G (TYRP1)
NM_000550.3:c.1395A>G (TYRP1) MANE Select NP_000541.1:p.Glu465=