Canonical Allele Identifier: CA1939984058
Gene: GRK5 HGNC NCBI
GRK5-IT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119211068_119211070delinsTTG , CM000672.2:g.119211068_119211070delinsTTG GRCh38
NC_000010.10:g.120970580_120970582delinsTTG , CM000672.1:g.120970580_120970582delinsTTG GRCh37
NC_000010.9:g.120960570_120960572delinsTTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000392870.3:c.52+3099_52+3101delinsTTG (GRK5) MANE Select ENSP00000376609.2:n.52+3099_52+3101delinsTTG
ENST00000392870.2:c.52+3099_52+3101delinsTTG (GRK5) ENSP00000376609.2:n.52+3099_52+3101delinsTTG
NM_005308.2:c.52+3099_52+3101delinsTTG (GRK5) NP_005299.1:n.52+3099_52+3101delinsTTG
XM_005269707.1:c.52+3099_52+3101delinsTTG (GRK5) XP_005269764.1:n.52+3099_52+3101delinsTTG
XM_005269708.1:c.52+3099_52+3101delinsTTG (GRK5) XP_005269765.1:n.52+3099_52+3101delinsTTG
XR_246196.2:n.583-413_583-411delinsTTG (GRK5-IT1)
XM_005269707.2:c.52+3099_52+3101delinsTTG (GRK5) XP_005269764.1:n.52+3099_52+3101delinsTTG
XR_246196.4:n.669-413_669-411delinsTTG (GRK5-IT1)
NM_005308.3:c.52+3099_52+3101delinsTTG (GRK5) MANE Select NP_005299.1:n.52+3099_52+3101delinsTTG