Canonical Allele Identifier: CA1703612863

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145540_44145567delinsTGCGCATTACGTCCTCGCTGCGGCTCTC , CM000669.2:g.44145540_44145567delinsTGCGCATTACGTCCTCGCTGCGGCTCTC	GRCh38
NC_000007.13:g.44185139_44185166delinsTGCGCATTACGTCCTCGCTGCGGCTCTC , CM000669.1:g.44185139_44185166delinsTGCGCATTACGTCCTCGCTGCGGCTCTC	GRCh37
NC_000007.12:g.44151664_44151691delinsTGCGCATTACGTCCTCGCTGCGGCTCTC	NCBI36
NG_008847.1:g.48857_48884delinsGAGAGCCGCAGCGAGGACGTAATGCGCA
NG_008847.2:g.57604_57631delinsGAGAGCCGCAGCGAGGACGTAATGCGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1181_*1208delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	ENSP00000379142.4:n.*1181_*1208delinsGAGAGCCGCAGCGAGGACGTAATG...
ENST00000616242.5:c.*303_*330delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	ENSP00000482149.2:n.*303_*330delinsGAGAGCCGCAGCGAGGACGTAATGCG...
ENST00000683378.1:n.409_436delinsGAGAGCCGCAGCGAGGACGTAATGCGCA
ENST00000336642.9:c.217_244delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	ENSP00000338009.5:p.Glu73=
ENST00000345378.7:c.1186_1213delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	ENSP00000223366.2:p.Glu396=
ENST00000403799.8:c.1183_1210delinsGAGAGCCGCAGCGAGGACGTAATGCGCA MANE Select	ENSP00000384247.3:p.Glu395=
ENST00000671824.1:c.1246_1273delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	ENSP00000500264.1:p.Glu416=
ENST00000672743.1:n.195_222delinsGAGAGCCGCAGCGAGGACGTAATGCGCA
ENST00000673284.1:c.1183_1210delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	ENSP00000499852.1:p.Glu395=
ENST00000336642.8:c.235_262delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	ENSP00000338009.4:p.Glu79=
ENST00000345378.6:c.1186_1213delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	ENSP00000223366.2:p.Glu396=
ENST00000395796.7:c.1180_1207delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	ENSP00000379142.3:p.Glu394=
ENST00000403799.7:c.1183_1210delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	ENSP00000384247.3:p.Glu395=
ENST00000437084.1:c.1132_1159delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	ENSP00000402840.1:p.Glu378=
ENST00000459642.1:n.563_590delinsGAGAGCCGCAGCGAGGACGTAATGCGCA
ENST00000616242.4:c.1180_1207delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	ENSP00000482149.1:p.Glu394=
NM_000162.3:c.1183_1210delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	NP_000153.1:p.Glu395=
NM_033507.1:c.1186_1213delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	NP_277042.1:p.Glu396=
NM_033508.1:c.1180_1207delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	NP_277043.1:p.Glu394=
NM_000162.4:c.1183_1210delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	NP_000153.1:p.Glu395=
NM_001354800.1:c.1183_1210delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	NP_001341729.1:p.Glu395=
NM_001354801.1:c.172_199delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	NP_001341730.1:p.Glu58=
NM_001354802.1:c.43_70delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	NP_001341731.1:p.Glu15=
NM_001354803.1:c.217_244delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	NP_001341732.1:p.Glu73=
NM_033507.2:c.1186_1213delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	NP_277042.1:p.Glu396=
NM_033508.2:c.1180_1207delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	NP_277043.1:p.Glu394=
XM_024446707.1:c.43_70delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	XP_024302475.1:p.Glu15=
NM_000162.5:c.1183_1210delinsGAGAGCCGCAGCGAGGACGTAATGCGCA MANE Select	NP_000153.1:p.Glu395=
NM_033507.3:c.1186_1213delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	NP_277042.1:p.Glu396=
NM_033508.3:c.1180_1207delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	NP_277043.1:p.Glu394=
NM_001354803.2:c.217_244delinsGAGAGCCGCAGCGAGGACGTAATGCGCA	NP_001341732.1:p.Glu73=