Canonical Allele Identifier: CA660614693

Gene: GRK5 GRK5-IT1

Linked Data

• dbSNP Id: rs1486909608
• MyVariant Identifiers: chr10:g.120969850_120969851del (hg19) ; chr10:g.119210338_119210339del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119210343_119210344del , CM000672.2:g.119210343_119210344del	GRCh38
NC_000010.10:g.120969855_120969856del , CM000672.1:g.120969855_120969856del	GRCh37
NC_000010.9:g.120959845_120959846del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392870.3:c.52+2374_52+2375del (GRK5) MANE Select	ENSP00000376609.2:n.52+2374_52+2375del
ENST00000392870.2:c.52+2374_52+2375del (GRK5)	ENSP00000376609.2:n.52+2374_52+2375del
NM_005308.2:c.52+2374_52+2375del (GRK5)	NP_005299.1:n.52+2374_52+2375del
XM_005269707.1:c.52+2374_52+2375del (GRK5)	XP_005269764.1:n.52+2374_52+2375del
XM_005269708.1:c.52+2374_52+2375del (GRK5)	XP_005269765.1:n.52+2374_52+2375del
XR_246196.2:n.583-1138_583-1137del (GRK5-IT1)
XM_005269707.2:c.52+2374_52+2375del (GRK5)	XP_005269764.1:n.52+2374_52+2375del
XR_246196.4:n.669-1138_669-1137del (GRK5-IT1)
NM_005308.3:c.52+2374_52+2375del (GRK5) MANE Select	NP_005299.1:n.52+2374_52+2375del