Canonical Allele Identifier: CA1703612668

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145194_44145195delinsCG , CM000669.2:g.44145194_44145195delinsCG	GRCh38
NC_000007.13:g.44184793_44184794delinsCG , CM000669.1:g.44184793_44184794delinsCG	GRCh37
NC_000007.12:g.44151318_44151319delinsCG	NCBI36
NG_008847.1:g.49229_49230delinsCG
NG_008847.2:g.57976_57977delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1337_*1338delinsCG	ENSP00000379142.4:n.*1337_*1338delinsCG
ENST00000616242.5:c.*459_*460delinsCG	ENSP00000482149.2:n.*459_*460delinsCG
ENST00000683378.1:n.565_566delinsCG
ENST00000336642.9:c.373_374delinsCG	ENSP00000338009.5:p.Arg125=
ENST00000345378.7:c.1342_1343delinsCG	ENSP00000223366.2:p.Arg448=
ENST00000403799.8:c.1339_1340delinsCG MANE Select	ENSP00000384247.3:p.Arg447=
ENST00000671824.1:c.1402_1403delinsCG	ENSP00000500264.1:p.Arg468=
ENST00000672743.1:n.351_352delinsCG
ENST00000673284.1:c.1339_1340delinsCG	ENSP00000499852.1:p.Arg447=
ENST00000336642.8:c.391_392delinsCG	ENSP00000338009.4:p.Arg131=
ENST00000345378.6:c.1342_1343delinsCG	ENSP00000223366.2:p.Arg448=
ENST00000395796.7:c.1336_1337delinsCG	ENSP00000379142.3:p.Arg446=
ENST00000403799.7:c.1339_1340delinsCG	ENSP00000384247.3:p.Arg447=
ENST00000437084.1:c.1288_1289delinsCG	ENSP00000402840.1:p.Arg430=
ENST00000459642.1:n.719_720delinsCG
ENST00000616242.4:c.1336_1337delinsCG	ENSP00000482149.1:p.Arg446=
NM_000162.3:c.1339_1340delinsCG	NP_000153.1:p.Arg447=
NM_033507.1:c.1342_1343delinsCG	NP_277042.1:p.Arg448=
NM_033508.1:c.1336_1337delinsCG	NP_277043.1:p.Arg446=
NM_000162.4:c.1339_1340delinsCG	NP_000153.1:p.Arg447=
NM_001354800.1:c.1339_1340delinsCG	NP_001341729.1:p.Arg447=
NM_001354801.1:c.328_329delinsCG	NP_001341730.1:p.Arg110=
NM_001354802.1:c.199_200delinsCG	NP_001341731.1:p.Arg67=
NM_001354803.1:c.373_374delinsCG	NP_001341732.1:p.Arg125=
NM_033507.2:c.1342_1343delinsCG	NP_277042.1:p.Arg448=
NM_033508.2:c.1336_1337delinsCG	NP_277043.1:p.Arg446=
XM_024446707.1:c.199_200delinsCG	XP_024302475.1:p.Arg67=
NM_000162.5:c.1339_1340delinsCG MANE Select	NP_000153.1:p.Arg447=
NM_033507.3:c.1342_1343delinsCG	NP_277042.1:p.Arg448=
NM_033508.3:c.1336_1337delinsCG	NP_277043.1:p.Arg446=
NM_001354803.2:c.373_374delinsCG	NP_001341732.1:p.Arg125=