Canonical Allele Identifier: CA214157936
Gene: GRK5 HGNC NCBI
GRK5-IT1 HGNC NCBI

Linked Data

dbSNP Id: rs752593650

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119211068_119211069dup , CM000672.2:g.119211068_119211069dup GRCh38
NC_000010.10:g.120970580_120970581dup , CM000672.1:g.120970580_120970581dup GRCh37
NC_000010.9:g.120960570_120960571dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000392870.3:c.52+3099_52+3100dup (GRK5) MANE Select ENSP00000376609.2:n.52+3099_52+3100dup
ENST00000392870.2:c.52+3099_52+3100dup (GRK5) ENSP00000376609.2:n.52+3099_52+3100dup
NM_005308.2:c.52+3099_52+3100dup (GRK5) NP_005299.1:n.52+3099_52+3100dup
XM_005269707.1:c.52+3099_52+3100dup (GRK5) XP_005269764.1:n.52+3099_52+3100dup
XM_005269708.1:c.52+3099_52+3100dup (GRK5) XP_005269765.1:n.52+3099_52+3100dup
XR_246196.2:n.583-413_583-412dup (GRK5-IT1)
XM_005269707.2:c.52+3099_52+3100dup (GRK5) XP_005269764.1:n.52+3099_52+3100dup
XR_246196.4:n.669-413_669-412dup (GRK5-IT1)
NM_005308.3:c.52+3099_52+3100dup (GRK5) MANE Select NP_005299.1:n.52+3099_52+3100dup