Canonical Allele Identifier: CA660614803

Gene: GRK5 GRK5-IT1

Linked Data

• dbSNP Id: rs1326837113
• MyVariant Identifiers: chr10:g.120970207_120970211del (hg19) ; chr10:g.119210695_119210699del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119210701_119210705del , CM000672.2:g.119210701_119210705del	GRCh38
NC_000010.10:g.120970213_120970217del , CM000672.1:g.120970213_120970217del	GRCh37
NC_000010.9:g.120960203_120960207del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392870.3:c.52+2732_52+2736del (GRK5) MANE Select	ENSP00000376609.2:n.52+2732_52+2736del
ENST00000392870.2:c.52+2732_52+2736del (GRK5)	ENSP00000376609.2:n.52+2732_52+2736del
NM_005308.2:c.52+2732_52+2736del (GRK5)	NP_005299.1:n.52+2732_52+2736del
XM_005269707.1:c.52+2732_52+2736del (GRK5)	XP_005269764.1:n.52+2732_52+2736del
XM_005269708.1:c.52+2732_52+2736del (GRK5)	XP_005269765.1:n.52+2732_52+2736del
XR_246196.2:n.583-780_583-776del (GRK5-IT1)
XM_005269707.2:c.52+2732_52+2736del (GRK5)	XP_005269764.1:n.52+2732_52+2736del
XR_246196.4:n.669-780_669-776del (GRK5-IT1)
NM_005308.3:c.52+2732_52+2736del (GRK5) MANE Select	NP_005299.1:n.52+2732_52+2736del