Canonical Allele Identifier: CA1939983894

Gene: GRK5 GRK5-IT1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119210615_119210618delinsAGTT , CM000672.2:g.119210615_119210618delinsAGTT	GRCh38
NC_000010.10:g.120970127_120970130delinsAGTT , CM000672.1:g.120970127_120970130delinsAGTT	GRCh37
NC_000010.9:g.120960117_120960120delinsAGTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392870.3:c.52+2646_52+2649delinsAGTT (GRK5) MANE Select	ENSP00000376609.2:n.52+2646_52+2649delinsAGTT
ENST00000392870.2:c.52+2646_52+2649delinsAGTT (GRK5)	ENSP00000376609.2:n.52+2646_52+2649delinsAGTT
NM_005308.2:c.52+2646_52+2649delinsAGTT (GRK5)	NP_005299.1:n.52+2646_52+2649delinsAGTT
XM_005269707.1:c.52+2646_52+2649delinsAGTT (GRK5)	XP_005269764.1:n.52+2646_52+2649delinsAGTT
XM_005269708.1:c.52+2646_52+2649delinsAGTT (GRK5)	XP_005269765.1:n.52+2646_52+2649delinsAGTT
XR_246196.2:n.583-866_583-863delinsAGTT (GRK5-IT1)
XM_005269707.2:c.52+2646_52+2649delinsAGTT (GRK5)	XP_005269764.1:n.52+2646_52+2649delinsAGTT
XR_246196.4:n.669-866_669-863delinsAGTT (GRK5-IT1)
NM_005308.3:c.52+2646_52+2649delinsAGTT (GRK5) MANE Select	NP_005299.1:n.52+2646_52+2649delinsAGTT