Canonical Allele Identifier: CA2580077165
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2034038
ClinVar RCV Id: RCV002867585

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145730_44145731delinsAA , CM000669.2:g.44145730_44145731delinsAA GRCh38
NC_000007.13:g.44185329_44185330delinsAA , CM000669.1:g.44185329_44185330delinsAA GRCh37
NC_000007.12:g.44151854_44151855delinsAA NCBI36
NG_008847.1:g.48693_48694delinsTT
NG_008847.2:g.57440_57441delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1018-1_*1018delinsTT
ENST00000616242.5:c.*140-1_*140delinsTT
ENST00000683378.1:n.246-1_246delinsTT
ENST00000336642.9:c.54-1_54delinsTT
ENST00000345378.7:c.1023-1_1023delinsTT
ENST00000403799.8:c.1020-1_1020delinsTT
ENST00000671824.1:c.1083-1_1083delinsTT
ENST00000672743.1:n.32-1_32delinsTT
ENST00000673284.1:c.1020-1_1020delinsTT
ENST00000336642.8:c.72-1_72delinsTT
ENST00000345378.6:c.1023-1_1023delinsTT
ENST00000395796.7:c.1017-1_1017delinsTT
ENST00000403799.7:c.1020-1_1020delinsTT
ENST00000437084.1:c.969-1_969delinsTT
ENST00000459642.1:n.399_400delinsTT
ENST00000473353.1:n.318-1_318delinsTT
ENST00000616242.4:c.1017-1_1017delinsTT
NM_000162.3:c.1020-1_1020delinsTT
NM_033507.1:c.1023-1_1023delinsTT
NM_033508.1:c.1017-1_1017delinsTT
NM_000162.4:c.1020-1_1020delinsTT
NM_001354800.1:c.1020-1_1020delinsTT
NM_001354801.1:c.9-1_9delinsTT
NM_001354802.1:c.-121-1_-121delinsTT
NM_001354803.1:c.54-1_54delinsTT
NM_033507.2:c.1023-1_1023delinsTT
NM_033508.2:c.1017-1_1017delinsTT
XM_024446707.1:c.-121-1_-121delinsTT
NM_000162.5:c.1020-1_1020delinsTT
NM_033507.3:c.1023-1_1023delinsTT
NM_033508.3:c.1017-1_1017delinsTT
NM_001354803.2:c.54-1_54delinsTT