Canonical Allele Identifier: CA2580612103
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145734_44145762del , CM000669.2:g.44145734_44145762del GRCh38
NC_000007.13:g.44185333_44185361del , CM000669.1:g.44185333_44185361del GRCh37
NC_000007.12:g.44151858_44151886del NCBI36
NG_008847.1:g.48669_48697del
NG_008847.2:g.57416_57444del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1018-25_*1021del
ENST00000616242.5:c.*140-25_*143del
ENST00000683378.1:n.246-25_249del
ENST00000336642.9:c.54-25_57del
ENST00000345378.7:c.1023-25_1026del
ENST00000403799.8:c.1020-25_1023del
ENST00000671824.1:c.1083-25_1086del
ENST00000672743.1:n.32-25_35del
ENST00000673284.1:c.1020-25_1023del
ENST00000336642.8:c.72-25_75del
ENST00000345378.6:c.1023-25_1026del
ENST00000395796.7:c.1017-25_1020del
ENST00000403799.7:c.1020-25_1023del
ENST00000437084.1:c.969-25_972del
ENST00000459642.1:n.375_403del
ENST00000473353.1:n.318-25_321del
ENST00000616242.4:c.1017-25_1020del
NM_000162.3:c.1020-25_1023del
NM_033507.1:c.1023-25_1026del
NM_033508.1:c.1017-25_1020del
NM_000162.4:c.1020-25_1023del
NM_001354800.1:c.1020-25_1023del
NM_001354801.1:c.9-25_12del
NM_001354802.1:c.-121-25_-118del
NM_001354803.1:c.54-25_57del
NM_033507.2:c.1023-25_1026del
NM_033508.2:c.1017-25_1020del
XM_024446707.1:c.-121-25_-118del
NM_000162.5:c.1020-25_1023del
NM_033507.3:c.1023-25_1026del
NM_033508.3:c.1017-25_1020del
NM_001354803.2:c.54-25_57del