Canonical Allele Identifier: CA1703613364

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146313_44146314delinsGC , CM000669.2:g.44146313_44146314delinsGC	GRCh38
NC_000007.13:g.44185912_44185913delinsGC , CM000669.1:g.44185912_44185913delinsGC	GRCh37
NC_000007.12:g.44152437_44152438delinsGC	NCBI36
NG_008847.1:g.48110_48111delinsGC
NG_008847.2:g.56857_56858delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1017+149_*1017+150delinsGC	ENSP00000379142.4:n.*1017+149_*1017+150delinsGC
ENST00000616242.5:c.*139+149_*139+150delinsGC	ENSP00000482149.2:n.*139+149_*139+150delinsGC
ENST00000683378.1:n.245+149_245+150delinsGC
ENST00000345378.7:c.1022+149_1022+150delinsGC	ENSP00000223366.2:n.1022+149_1022+150delinsGC
ENST00000403799.8:c.1019+149_1019+150delinsGC MANE Select	ENSP00000384247.3:n.1019+149_1019+150delinsGC
ENST00000671824.1:c.1082+149_1082+150delinsGC	ENSP00000500264.1:n.1082+149_1082+150delinsGC
ENST00000673284.1:c.1019+149_1019+150delinsGC	ENSP00000499852.1:n.1019+149_1019+150delinsGC
ENST00000345378.6:c.1022+149_1022+150delinsGC	ENSP00000223366.2:n.1022+149_1022+150delinsGC
ENST00000395796.7:c.1016+149_1016+150delinsGC	ENSP00000379142.3:n.1016+149_1016+150delinsGC
ENST00000403799.7:c.1019+149_1019+150delinsGC	ENSP00000384247.3:n.1019+149_1019+150delinsGC
ENST00000437084.1:c.968+149_968+150delinsGC	ENSP00000402840.1:n.968+149_968+150delinsGC
ENST00000473353.1:n.317+149_317+150delinsGC
ENST00000616242.4:c.1016+149_1016+150delinsGC	ENSP00000482149.1:n.1016+149_1016+150delinsGC
NM_000162.3:c.1019+149_1019+150delinsGC	NP_000153.1:n.1019+149_1019+150delinsGC
NM_033507.1:c.1022+149_1022+150delinsGC	NP_277042.1:n.1022+149_1022+150delinsGC
NM_033508.1:c.1016+149_1016+150delinsGC	NP_277043.1:n.1016+149_1016+150delinsGC
NM_000162.4:c.1019+149_1019+150delinsGC	NP_000153.1:n.1019+149_1019+150delinsGC
NM_001354800.1:c.1019+149_1019+150delinsGC	NP_001341729.1:n.1019+149_1019+150delinsGC
NM_001354801.1:c.8+305_8+306delinsGC	NP_001341730.1:n.8+305_8+306delinsGC
NM_033507.2:c.1022+149_1022+150delinsGC	NP_277042.1:n.1022+149_1022+150delinsGC
NM_033508.2:c.1016+149_1016+150delinsGC	NP_277043.1:n.1016+149_1016+150delinsGC
NM_000162.5:c.1019+149_1019+150delinsGC MANE Select	NP_000153.1:n.1019+149_1019+150delinsGC
NM_033507.3:c.1022+149_1022+150delinsGC	NP_277042.1:n.1022+149_1022+150delinsGC
NM_033508.3:c.1016+149_1016+150delinsGC	NP_277043.1:n.1016+149_1016+150delinsGC