Canonical Allele Identifier: CA1703612656

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145173_44145174delinsGC , CM000669.2:g.44145173_44145174delinsGC	GRCh38
NC_000007.13:g.44184772_44184773delinsGC , CM000669.1:g.44184772_44184773delinsGC	GRCh37
NC_000007.12:g.44151297_44151298delinsGC	NCBI36
NG_008847.1:g.49250_49251delinsGC
NG_008847.2:g.57997_57998delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1358_*1359delinsGC	ENSP00000379142.4:n.*1358_*1359delinsGC
ENST00000616242.5:c.*480_*481delinsGC	ENSP00000482149.2:n.*480_*481delinsGC
ENST00000683378.1:n.586_587delinsGC
ENST00000336642.9:c.394_395delinsGC	ENSP00000338009.5:p.Ala132=
ENST00000345378.7:c.1363_1364delinsGC	ENSP00000223366.2:p.Ala455=
ENST00000403799.8:c.1360_1361delinsGC MANE Select	ENSP00000384247.3:p.Ala454=
ENST00000671824.1:c.1423_1424delinsGC	ENSP00000500264.1:p.Ala475=
ENST00000672743.1:n.372_373delinsGC
ENST00000673284.1:c.1360_1361delinsGC	ENSP00000499852.1:p.Ala454=
ENST00000336642.8:c.412_413delinsGC	ENSP00000338009.4:p.Ala138=
ENST00000345378.6:c.1363_1364delinsGC	ENSP00000223366.2:p.Ala455=
ENST00000395796.7:c.1357_1358delinsGC	ENSP00000379142.3:p.Ala453=
ENST00000403799.7:c.1360_1361delinsGC	ENSP00000384247.3:p.Ala454=
ENST00000437084.1:c.1309_1310delinsGC	ENSP00000402840.1:p.Ala437=
ENST00000459642.1:n.740_741delinsGC
ENST00000616242.4:c.1357_1358delinsGC	ENSP00000482149.1:p.Ala453=
NM_000162.3:c.1360_1361delinsGC	NP_000153.1:p.Ala454=
NM_033507.1:c.1363_1364delinsGC	NP_277042.1:p.Ala455=
NM_033508.1:c.1357_1358delinsGC	NP_277043.1:p.Ala453=
NM_000162.4:c.1360_1361delinsGC	NP_000153.1:p.Ala454=
NM_001354800.1:c.1360_1361delinsGC	NP_001341729.1:p.Ala454=
NM_001354801.1:c.349_350delinsGC	NP_001341730.1:p.Ala117=
NM_001354802.1:c.220_221delinsGC	NP_001341731.1:p.Ala74=
NM_001354803.1:c.394_395delinsGC	NP_001341732.1:p.Ala132=
NM_033507.2:c.1363_1364delinsGC	NP_277042.1:p.Ala455=
NM_033508.2:c.1357_1358delinsGC	NP_277043.1:p.Ala453=
XM_024446707.1:c.220_221delinsGC	XP_024302475.1:p.Ala74=
NM_000162.5:c.1360_1361delinsGC MANE Select	NP_000153.1:p.Ala454=
NM_033507.3:c.1363_1364delinsGC	NP_277042.1:p.Ala455=
NM_033508.3:c.1357_1358delinsGC	NP_277043.1:p.Ala453=
NM_001354803.2:c.394_395delinsGC	NP_001341732.1:p.Ala132=