Canonical Allele Identifier: CA1939983838
Gene: GRK5 HGNC NCBI
GRK5-IT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119210443_119210444delinsCT , CM000672.2:g.119210443_119210444delinsCT GRCh38
NC_000010.10:g.120969955_120969956delinsCT , CM000672.1:g.120969955_120969956delinsCT GRCh37
NC_000010.9:g.120959945_120959946delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392870.3:c.52+2474_52+2475delinsCT (GRK5) MANE Select ENSP00000376609.2:n.52+2474_52+2475delins...
ENST00000392870.2:c.52+2474_52+2475delinsCT (GRK5) ENSP00000376609.2:n.52+2474_52+2475delins...
NM_005308.2:c.52+2474_52+2475delinsCT (GRK5) NP_005299.1:n.52+2474_52+2475delinsCT
XM_005269707.1:c.52+2474_52+2475delinsCT (GRK5) XP_005269764.1:n.52+2474_52+2475delinsCT
XM_005269708.1:c.52+2474_52+2475delinsCT (GRK5) XP_005269765.1:n.52+2474_52+2475delinsCT
XR_246196.2:n.583-1038_583-1037delinsCT (GRK5-IT1)
XM_005269707.2:c.52+2474_52+2475delinsCT (GRK5) XP_005269764.1:n.52+2474_52+2475delinsCT
XR_246196.4:n.669-1038_669-1037delinsCT (GRK5-IT1)
NM_005308.3:c.52+2474_52+2475delinsCT (GRK5) MANE Select NP_005299.1:n.52+2474_52+2475delinsCT