Canonical Allele Identifier: CA463860385
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

gnomAD v4: 9-12704687-C-T
MyVariant Identifiers: chr9:g.12704687C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12704687C>T , CM000671.2:g.12704687C>T GRCh38
NC_000009.11:g.12704687C>T , CM000671.1:g.12704687C>T GRCh37
NC_000009.10:g.12694687C>T NCBI36
NG_011705.1:g.16302C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.1243C>T (TYRP1) MANE Select ENSP00000373570.4:p.Leu415=
ENST00000381136.2:c.373C>T (TYRP1) ENSP00000370528.2:p.Leu125=
ENST00000381142.3:n.480C>T (TYRP1)
ENST00000388918.9:c.1243C>T (TYRP1) ENSP00000373570.4:p.Leu415=
NM_000550.2:c.1243C>T (TYRP1) NP_000541.1:p.Leu415=
NR_125775.1:n.317-4061G>A (LURAP1L-AS1)
XR_001746372.2:n.1227C>T (TYRP1)
NM_000550.3:c.1243C>T (TYRP1) MANE Select NP_000541.1:p.Leu415=