Canonical Allele Identifier: CA1703612698

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145249_44145251delinsTGC , CM000669.2:g.44145249_44145251delinsTGC	GRCh38
NC_000007.13:g.44184848_44184850delinsTGC , CM000669.1:g.44184848_44184850delinsTGC	GRCh37
NC_000007.12:g.44151373_44151375delinsTGC	NCBI36
NG_008847.1:g.49173_49175delinsGCA
NG_008847.2:g.57920_57922delinsGCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1281_*1283delinsGCA	ENSP00000379142.4:n.*1281_*1283delinsGCA
ENST00000616242.5:c.*403_*405delinsGCA	ENSP00000482149.2:n.*403_*405delinsGCA
ENST00000683378.1:n.509_511delinsGCA
ENST00000336642.9:c.317_319delinsGCA	ENSP00000338009.5:p.Arg106=
ENST00000345378.7:c.1286_1288delinsGCA	ENSP00000223366.2:p.Arg429=
ENST00000403799.8:c.1283_1285delinsGCA MANE Select	ENSP00000384247.3:p.Arg428=
ENST00000671824.1:c.1346_1348delinsGCA	ENSP00000500264.1:p.Arg449=
ENST00000672743.1:n.295_297delinsGCA
ENST00000673284.1:c.1283_1285delinsGCA	ENSP00000499852.1:p.Arg428=
ENST00000336642.8:c.335_337delinsGCA	ENSP00000338009.4:p.Arg112=
ENST00000345378.6:c.1286_1288delinsGCA	ENSP00000223366.2:p.Arg429=
ENST00000395796.7:c.1280_1282delinsGCA	ENSP00000379142.3:p.Arg427=
ENST00000403799.7:c.1283_1285delinsGCA	ENSP00000384247.3:p.Arg428=
ENST00000437084.1:c.1232_1234delinsGCA	ENSP00000402840.1:p.Arg411=
ENST00000459642.1:n.663_665delinsGCA
ENST00000616242.4:c.1280_1282delinsGCA	ENSP00000482149.1:p.Arg427=
NM_000162.3:c.1283_1285delinsGCA	NP_000153.1:p.Arg428=
NM_033507.1:c.1286_1288delinsGCA	NP_277042.1:p.Arg429=
NM_033508.1:c.1280_1282delinsGCA	NP_277043.1:p.Arg427=
NM_000162.4:c.1283_1285delinsGCA	NP_000153.1:p.Arg428=
NM_001354800.1:c.1283_1285delinsGCA	NP_001341729.1:p.Arg428=
NM_001354801.1:c.272_274delinsGCA	NP_001341730.1:p.Arg91=
NM_001354802.1:c.143_145delinsGCA	NP_001341731.1:p.Arg48=
NM_001354803.1:c.317_319delinsGCA	NP_001341732.1:p.Arg106=
NM_033507.2:c.1286_1288delinsGCA	NP_277042.1:p.Arg429=
NM_033508.2:c.1280_1282delinsGCA	NP_277043.1:p.Arg427=
XM_024446707.1:c.143_145delinsGCA	XP_024302475.1:p.Arg48=
NM_000162.5:c.1283_1285delinsGCA MANE Select	NP_000153.1:p.Arg428=
NM_033507.3:c.1286_1288delinsGCA	NP_277042.1:p.Arg429=
NM_033508.3:c.1280_1282delinsGCA	NP_277043.1:p.Arg427=
NM_001354803.2:c.317_319delinsGCA	NP_001341732.1:p.Arg106=