Canonical Allele Identifier: CA1939983921
Gene: GRK5 HGNC NCBI
GRK5-IT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119210693_119210694delinsGA , CM000672.2:g.119210693_119210694delinsGA GRCh38
NC_000010.10:g.120970205_120970206delinsGA , CM000672.1:g.120970205_120970206delinsGA GRCh37
NC_000010.9:g.120960195_120960196delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000392870.3:c.52+2724_52+2725delinsGA (GRK5) MANE Select ENSP00000376609.2:n.52+2724_52+2725delinsGA
ENST00000392870.2:c.52+2724_52+2725delinsGA (GRK5) ENSP00000376609.2:n.52+2724_52+2725delinsGA
NM_005308.2:c.52+2724_52+2725delinsGA (GRK5) NP_005299.1:n.52+2724_52+2725delinsGA
XM_005269707.1:c.52+2724_52+2725delinsGA (GRK5) XP_005269764.1:n.52+2724_52+2725delinsGA
XM_005269708.1:c.52+2724_52+2725delinsGA (GRK5) XP_005269765.1:n.52+2724_52+2725delinsGA
XR_246196.2:n.583-788_583-787delinsGA (GRK5-IT1)
XM_005269707.2:c.52+2724_52+2725delinsGA (GRK5) XP_005269764.1:n.52+2724_52+2725delinsGA
XR_246196.4:n.669-788_669-787delinsGA (GRK5-IT1)
NM_005308.3:c.52+2724_52+2725delinsGA (GRK5) MANE Select NP_005299.1:n.52+2724_52+2725delinsGA