Canonical Allele Identifier: CA463860190
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.12702431A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12702431A>C , CM000671.2:g.12702431A>C GRCh38
NC_000009.11:g.12702431A>C , CM000671.1:g.12702431A>C GRCh37
NC_000009.10:g.12692431A>C NCBI36
NG_011705.1:g.14046A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.1074A>C (TYRP1) MANE Select ENSP00000373570.4:p.Thr358=
ENST00000381136.2:c.204A>C (TYRP1) ENSP00000370528.2:p.Thr68=
ENST00000381142.3:n.311A>C (TYRP1)
ENST00000388918.9:c.1074A>C (TYRP1) ENSP00000373570.4:p.Thr358=
ENST00000470909.1:n.332A>C (TYRP1)
NM_000550.2:c.1074A>C (TYRP1) NP_000541.1:p.Thr358=
NR_125775.1:n.317-1805T>G (LURAP1L-AS1)
XR_001746372.2:n.1058A>C (TYRP1)
NM_000550.3:c.1074A>C (TYRP1) MANE Select NP_000541.1:p.Thr358=