Canonical Allele Identifier: CA596301335

Gene: GRK5 GRK5-IT1

Linked Data

• dbSNP Id: rs1266682317
• gnomAD v2: 10-120970517-G-A
• gnomAD v3: 10-119211005-G-A
• gnomAD v4: 10-119211005-G-A
• MyVariant Identifiers: chr10:g.120970517G>A (hg19) ; chr10:g.119211005G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119211005G>A , CM000672.2:g.119211005G>A	GRCh38
NC_000010.10:g.120970517G>A , CM000672.1:g.120970517G>A	GRCh37
NC_000010.9:g.120960507G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392870.3:c.52+3036G>A (GRK5) MANE Select	ENSP00000376609.2:n.52+3036G>A
ENST00000392870.2:c.52+3036G>A (GRK5)	ENSP00000376609.2:n.52+3036G>A
NM_005308.2:c.52+3036G>A (GRK5)	NP_005299.1:n.52+3036G>A
XM_005269707.1:c.52+3036G>A (GRK5)	XP_005269764.1:n.52+3036G>A
XM_005269708.1:c.52+3036G>A (GRK5)	XP_005269765.1:n.52+3036G>A
XR_246196.2:n.583-476G>A (GRK5-IT1)
XM_005269707.2:c.52+3036G>A (GRK5)	XP_005269764.1:n.52+3036G>A
XR_246196.4:n.669-476G>A (GRK5-IT1)
NM_005308.3:c.52+3036G>A (GRK5) MANE Select	NP_005299.1:n.52+3036G>A