Canonical Allele Identifier: CA660614901

Gene: GRK5 GRK5-IT1

Linked Data

• dbSNP Id: rs1376557994
• gnomAD v3: 10-119211046-A-G
• gnomAD v4: 10-119211046-A-G
• MyVariant Identifiers: chr10:g.120970558A>G (hg19) ; chr10:g.119211046A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119211046A>G , CM000672.2:g.119211046A>G	GRCh38
NC_000010.10:g.120970558A>G , CM000672.1:g.120970558A>G	GRCh37
NC_000010.9:g.120960548A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392870.3:c.52+3077A>G (GRK5) MANE Select	ENSP00000376609.2:n.52+3077A>G
ENST00000392870.2:c.52+3077A>G (GRK5)	ENSP00000376609.2:n.52+3077A>G
NM_005308.2:c.52+3077A>G (GRK5)	NP_005299.1:n.52+3077A>G
XM_005269707.1:c.52+3077A>G (GRK5)	XP_005269764.1:n.52+3077A>G
XM_005269708.1:c.52+3077A>G (GRK5)	XP_005269765.1:n.52+3077A>G
XR_246196.2:n.583-435A>G (GRK5-IT1)
XM_005269707.2:c.52+3077A>G (GRK5)	XP_005269764.1:n.52+3077A>G
XR_246196.4:n.669-435A>G (GRK5-IT1)
NM_005308.3:c.52+3077A>G (GRK5) MANE Select	NP_005299.1:n.52+3077A>G