Canonical Allele Identifier: CA10632559
Gene: TYRP1 HGNC NCBI
LURAP1L-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 364866
ClinVar RCV Id: RCV000394515
dbSNP Id: rs549032453
gnomAD v2: 9-12709640-A-G
gnomAD v3: 9-12709640-A-G
gnomAD v4: 9-12709640-A-G
MyVariant Identifiers: chr9:g.12709640A>G (hg19) chr9:g.12709640A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12709640A>G , CM000671.2:g.12709640A>G GRCh38
NC_000009.11:g.12709640A>G , CM000671.1:g.12709640A>G GRCh37
NC_000009.10:g.12699640A>G NCBI36
NG_011705.1:g.21255A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000388918.10:c.*458A>G (TYRP1) MANE Select ENSP00000373570.4:n.*458A>G
ENST00000388918.9:c.*458A>G (TYRP1) ENSP00000373570.4:n.*458A>G
NM_000550.2:c.*458A>G (TYRP1) NP_000541.1:n.*458A>G
NR_125775.1:n.317-9014T>C (LURAP1L-AS1)
XR_001746372.2:n.2056A>G (TYRP1)
NM_000550.3:c.*458A>G (TYRP1) MANE Select NP_000541.1:n.*458A>G
Search 100 bp 5'
Search 100 bp 3'