Canonical Allele Identifier: CA2695202954

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145191_44145194delinsAGACCAG , CM000669.2:g.44145191_44145194delinsAGACCAG	GRCh38
NC_000007.13:g.44184790_44184793delinsAGACCAG , CM000669.1:g.44184790_44184793delinsAGACCAG	GRCh37
NC_000007.12:g.44151315_44151318delinsAGACCAG	NCBI36
NG_008847.1:g.49230_49233delinsCTGGTCT
NG_008847.2:g.57977_57980delinsCTGGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1338_*1341delinsCTGGTCT	ENSP00000379142.4:n.*1338_*1341delinsCTGGTCT
ENST00000616242.5:c.*460_*463delinsCTGGTCT	ENSP00000482149.2:n.*460_*463delinsCTGGTCT
ENST00000683378.1:n.566_569delinsCTGGTCT
ENST00000336642.9:c.374_377delinsCTGGTCT	ENSP00000338009.5:p.Arg125_Gly126delinsProGlyLeu
ENST00000345378.7:c.1343_1346delinsCTGGTCT	ENSP00000223366.2:p.Arg448_Gly449delinsProGlyLeu
ENST00000403799.8:c.1340_1343delinsCTGGTCT MANE Select	ENSP00000384247.3:p.Arg447_Gly448delinsProGlyLeu
ENST00000671824.1:c.1403_1406delinsCTGGTCT	ENSP00000500264.1:p.Arg468_Gly469delinsProGlyLeu
ENST00000672743.1:n.352_355delinsCTGGTCT
ENST00000673284.1:c.1340_1343delinsCTGGTCT	ENSP00000499852.1:p.Arg447_Gly448delinsProGlyLeu
ENST00000336642.8:c.392_395delinsCTGGTCT	ENSP00000338009.4:p.Arg131_Gly132delinsProGlyLeu
ENST00000345378.6:c.1343_1346delinsCTGGTCT	ENSP00000223366.2:p.Arg448_Gly449delinsProGlyLeu
ENST00000395796.7:c.1337_1340delinsCTGGTCT	ENSP00000379142.3:p.Arg446_Gly447delinsProGlyLeu
ENST00000403799.7:c.1340_1343delinsCTGGTCT	ENSP00000384247.3:p.Arg447_Gly448delinsProGlyLeu
ENST00000437084.1:c.1289_1292delinsCTGGTCT	ENSP00000402840.1:p.Arg430_Gly431delinsProGlyLeu
ENST00000459642.1:n.720_723delinsCTGGTCT
ENST00000616242.4:c.1337_1340delinsCTGGTCT	ENSP00000482149.1:p.Arg446_Gly447delinsProGlyLeu
NM_000162.3:c.1340_1343delinsCTGGTCT	NP_000153.1:p.Arg447_Gly448delinsProGlyLeu
NM_033507.1:c.1343_1346delinsCTGGTCT	NP_277042.1:p.Arg448_Gly449delinsProGlyLeu
NM_033508.1:c.1337_1340delinsCTGGTCT	NP_277043.1:p.Arg446_Gly447delinsProGlyLeu
NM_000162.4:c.1340_1343delinsCTGGTCT	NP_000153.1:p.Arg447_Gly448delinsProGlyLeu
NM_001354800.1:c.1340_1343delinsCTGGTCT	NP_001341729.1:p.Arg447_Gly448delinsProGlyLeu
NM_001354801.1:c.329_332delinsCTGGTCT	NP_001341730.1:p.Arg110_Gly111delinsProGlyLeu
NM_001354802.1:c.200_203delinsCTGGTCT	NP_001341731.1:p.Arg67_Gly68delinsProGlyLeu
NM_001354803.1:c.374_377delinsCTGGTCT	NP_001341732.1:p.Arg125_Gly126delinsProGlyLeu
NM_033507.2:c.1343_1346delinsCTGGTCT	NP_277042.1:p.Arg448_Gly449delinsProGlyLeu
NM_033508.2:c.1337_1340delinsCTGGTCT	NP_277043.1:p.Arg446_Gly447delinsProGlyLeu
XM_024446707.1:c.200_203delinsCTGGTCT	XP_024302475.1:p.Arg67_Gly68delinsProGlyLeu
NM_000162.5:c.1340_1343delinsCTGGTCT MANE Select	NP_000153.1:p.Arg447_Gly448delinsProGlyLeu
NM_033507.3:c.1343_1346delinsCTGGTCT	NP_277042.1:p.Arg448_Gly449delinsProGlyLeu
NM_033508.3:c.1337_1340delinsCTGGTCT	NP_277043.1:p.Arg446_Gly447delinsProGlyLeu
NM_001354803.2:c.374_377delinsCTGGTCT	NP_001341732.1:p.Arg125_Gly126delinsProGlyLeu