Canonical Allele Identifier: CA2695203055
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145719_44145741del , CM000669.2:g.44145719_44145741del GRCh38
NC_000007.13:g.44185318_44185340del , CM000669.1:g.44185318_44185340del GRCh37
NC_000007.12:g.44151843_44151865del NCBI36
NG_008847.1:g.48687_48709del
NG_008847.2:g.57434_57456del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1018-7_*1033del
ENST00000616242.5:c.*140-7_*155del
ENST00000683378.1:n.246-7_261del
ENST00000336642.9:c.54-7_69del
ENST00000345378.7:c.1023-7_1038del
ENST00000403799.8:c.1020-7_1035del
ENST00000671824.1:c.1083-7_1098del
ENST00000672743.1:n.32-7_47del
ENST00000673284.1:c.1020-7_1035del
ENST00000336642.8:c.72-7_87del
ENST00000345378.6:c.1023-7_1038del
ENST00000395796.7:c.1017-7_1032del
ENST00000403799.7:c.1020-7_1035del
ENST00000437084.1:c.969-7_984del
ENST00000459642.1:n.393_415del
ENST00000473353.1:n.318-7_333del
ENST00000616242.4:c.1017-7_1032del
NM_000162.3:c.1020-7_1035del
NM_033507.1:c.1023-7_1038del
NM_033508.1:c.1017-7_1032del
NM_000162.4:c.1020-7_1035del
NM_001354800.1:c.1020-7_1035del
NM_001354801.1:c.9-7_24del
NM_001354802.1:c.-121-7_-106del
NM_001354803.1:c.54-7_69del
NM_033507.2:c.1023-7_1038del
NM_033508.2:c.1017-7_1032del
XM_024446707.1:c.-121-7_-106del
NM_000162.5:c.1020-7_1035del
NM_033507.3:c.1023-7_1038del
NM_033508.3:c.1017-7_1032del
NM_001354803.2:c.54-7_69del