Canonical Allele Identifier: CA10628996
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 364865
ClinVar RCV Id: RCV000341603
dbSNP Id: rs2762464
gnomAD v2: 9-12709586-A-T
gnomAD v3: 9-12709586-A-T
gnomAD v4: 9-12709586-A-T
MyVariant Identifiers: chr9:g.12709586A>T (hg19) chr9:g.12709586A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12709586A>T , CM000671.2:g.12709586A>T GRCh38
NC_000009.11:g.12709586A>T , CM000671.1:g.12709586A>T GRCh37
NC_000009.10:g.12699586A>T NCBI36
NG_011705.1:g.21201A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.*404A>T (TYRP1) MANE Select ENSP00000373570.4:n.*404A>T
ENST00000388918.9:c.*404A>T (TYRP1) ENSP00000373570.4:n.*404A>T
NM_000550.2:c.*404A>T (TYRP1) NP_000541.1:n.*404A>T
NR_125775.1:n.317-8960T>A (LURAP1L-AS1)
XR_001746372.2:n.2002A>T (TYRP1)
NM_000550.3:c.*404A>T (TYRP1) MANE Select NP_000541.1:n.*404A>T
Search 100 bp 5'
Search 100 bp 3'