Canonical Allele Identifier: CA2580077164
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2443578
ClinVar RCV Id: RCV003152185

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145733_44145771del , CM000669.2:g.44145733_44145771del GRCh38
NC_000007.13:g.44185332_44185370del , CM000669.1:g.44185332_44185370del GRCh37
NC_000007.12:g.44151857_44151895del NCBI36
NG_008847.1:g.48661_48699del
NG_008847.2:g.57408_57446del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1018-33_*1023del
ENST00000616242.5:c.*140-33_*145del
ENST00000683378.1:n.246-33_251del
ENST00000336642.9:c.54-33_59del
ENST00000345378.7:c.1023-33_1028del
ENST00000403799.8:c.1020-33_1025del
ENST00000671824.1:c.1083-33_1088del
ENST00000672743.1:n.32-33_37del
ENST00000673284.1:c.1020-33_1025del
ENST00000336642.8:c.72-33_77del
ENST00000345378.6:c.1023-33_1028del
ENST00000395796.7:c.1017-33_1022del
ENST00000403799.7:c.1020-33_1025del
ENST00000437084.1:c.969-33_974del
ENST00000459642.1:n.367_405del
ENST00000473353.1:n.318-33_323del
ENST00000616242.4:c.1017-33_1022del
NM_000162.3:c.1020-33_1025del
NM_033507.1:c.1023-33_1028del
NM_033508.1:c.1017-33_1022del
NM_000162.4:c.1020-33_1025del
NM_001354800.1:c.1020-33_1025del
NM_001354801.1:c.9-33_14del
NM_001354802.1:c.-121-33_-116del
NM_001354803.1:c.54-33_59del
NM_033507.2:c.1023-33_1028del
NM_033508.2:c.1017-33_1022del
XM_024446707.1:c.-121-33_-116del
NM_000162.5:c.1020-33_1025del
NM_033507.3:c.1023-33_1028del
NM_033508.3:c.1017-33_1022del
NM_001354803.2:c.54-33_59del