Canonical Allele Identifier: CA4985491

Gene: TYRP1 LURAP1L-AS1

Linked Data

• ClinVar Variation Id: 2993993
• ClinVar RCV Id: RCV003853568
• dbSNP Id: rs776115420
• ExAC: 9:12704723 G / A
• gnomAD v2: 9-12704723-G-A
• gnomAD v3: 9-12704723-G-A
• gnomAD v4: 9-12704723-G-A
• MyVariant Identifiers: chr9:g.12704723G>A (hg19) ; chr9:g.12704723G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.12704723G>A , CM000671.2:g.12704723G>A	GRCh38
NC_000009.11:g.12704723G>A , CM000671.1:g.12704723G>A	GRCh37
NC_000009.10:g.12694723G>A	NCBI36
NG_011705.1:g.16338G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388918.10:c.1261+18G>A (TYRP1) MANE Select	ENSP00000373570.4:n.1261+18G>A
ENST00000381136.2:c.391+18G>A (TYRP1)	ENSP00000370528.2:n.391+18G>A
ENST00000381142.3:n.498+18G>A (TYRP1)
ENST00000388918.9:c.1261+18G>A (TYRP1)	ENSP00000373570.4:n.1261+18G>A
NM_000550.2:c.1261+18G>A (TYRP1)	NP_000541.1:n.1261+18G>A
NR_125775.1:n.317-4097C>T (LURAP1L-AS1)
XR_001746372.2:n.1245+18G>A (TYRP1)
NM_000550.3:c.1261+18G>A (TYRP1) MANE Select	NP_000541.1:n.1261+18G>A