Canonical Allele Identifier: CA2682582270
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145805_44145854del , CM000669.2:g.44145805_44145854del GRCh38
NC_000007.13:g.44185404_44185453del , CM000669.1:g.44185404_44185453del GRCh37
NC_000007.12:g.44151929_44151978del NCBI36
NG_008847.1:g.48585_48634del
NG_008847.2:g.57332_57381del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1018-109_*1018-60del ENSP00000379142.4:n.*1018-109_*1018-60del
ENST00000616242.5:c.*140-109_*140-60del ENSP00000482149.2:n.*140-109_*140-60del
ENST00000683378.1:n.246-109_246-60del
ENST00000336642.9:c.54-109_54-60del ENSP00000338009.5:n.54-109_54-60del
ENST00000345378.7:c.1023-109_1023-60del ENSP00000223366.2:n.1023-109_1023-60del
ENST00000403799.8:c.1020-109_1020-60del MANE Select ENSP00000384247.3:n.1020-109_1020-60del
ENST00000671824.1:c.1083-109_1083-60del ENSP00000500264.1:n.1083-109_1083-60del
ENST00000672743.1:n.31+70_32-60del
ENST00000673284.1:c.1020-109_1020-60del ENSP00000499852.1:n.1020-109_1020-60del
ENST00000336642.8:c.72-109_72-60del ENSP00000338009.4:n.72-109_72-60del
ENST00000345378.6:c.1023-109_1023-60del ENSP00000223366.2:n.1023-109_1023-60del
ENST00000395796.7:c.1017-109_1017-60del ENSP00000379142.3:n.1017-109_1017-60del
ENST00000403799.7:c.1020-109_1020-60del ENSP00000384247.3:n.1020-109_1020-60del
ENST00000437084.1:c.969-109_969-60del ENSP00000402840.1:n.969-109_969-60del
ENST00000459642.1:n.291_340del
ENST00000473353.1:n.318-109_318-60del
ENST00000616242.4:c.1017-109_1017-60del ENSP00000482149.1:n.1017-109_1017-60del
NM_000162.3:c.1020-109_1020-60del NP_000153.1:n.1020-109_1020-60del
NM_033507.1:c.1023-109_1023-60del NP_277042.1:n.1023-109_1023-60del
NM_033508.1:c.1017-109_1017-60del NP_277043.1:n.1017-109_1017-60del
NM_000162.4:c.1020-109_1020-60del NP_000153.1:n.1020-109_1020-60del
NM_001354800.1:c.1020-109_1020-60del NP_001341729.1:n.1020-109_1020-60del
NM_001354801.1:c.9-109_9-60del NP_001341730.1:n.9-109_9-60del
NM_001354802.1:c.-122+70_-121-60del NP_001341731.1:n.-122+70_-121-60del
NM_001354803.1:c.54-109_54-60del NP_001341732.1:n.54-109_54-60del
NM_033507.2:c.1023-109_1023-60del NP_277042.1:n.1023-109_1023-60del
NM_033508.2:c.1017-109_1017-60del NP_277043.1:n.1017-109_1017-60del
XM_024446707.1:c.-122+70_-121-60del XP_024302475.1:n.-122+70_-121-60del
NM_000162.5:c.1020-109_1020-60del MANE Select NP_000153.1:n.1020-109_1020-60del
NM_033507.3:c.1023-109_1023-60del NP_277042.1:n.1023-109_1023-60del
NM_033508.3:c.1017-109_1017-60del NP_277043.1:n.1017-109_1017-60del
NM_001354803.2:c.54-109_54-60del NP_001341732.1:n.54-109_54-60del