Canonical Allele Identifier: CA463860377
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2118259310
MyVariant Identifiers: chr9:g.12704677T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12704677T>C , CM000671.2:g.12704677T>C GRCh38
NC_000009.11:g.12704677T>C , CM000671.1:g.12704677T>C GRCh37
NC_000009.10:g.12694677T>C NCBI36
NG_011705.1:g.16292T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.1233T>C (TYRP1) MANE Select ENSP00000373570.4:p.Phe411=
ENST00000381136.2:c.363T>C (TYRP1) ENSP00000370528.2:p.Phe121=
ENST00000381142.3:n.470T>C (TYRP1)
ENST00000388918.9:c.1233T>C (TYRP1) ENSP00000373570.4:p.Phe411=
NM_000550.2:c.1233T>C (TYRP1) NP_000541.1:p.Phe411=
NR_125775.1:n.317-4051A>G (LURAP1L-AS1)
XR_001746372.2:n.1217T>C (TYRP1)
NM_000550.3:c.1233T>C (TYRP1) MANE Select NP_000541.1:p.Phe411=