Canonical Allele Identifier: CA2775232030

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146179_44146180insCCG , CM000669.2:g.44146179_44146180insCCG	GRCh38
NC_000007.13:g.44185778_44185779insCCG , CM000669.1:g.44185778_44185779insCCG	GRCh37
NC_000007.12:g.44152303_44152304insCCG	NCBI36
NG_008847.1:g.48244_48245insCGG
NG_008847.2:g.56991_56992insCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1017+283_*1017+284insCGG	ENSP00000379142.4:n.*1017+283_*1017+284insCGG
ENST00000616242.5:c.*139+283_*139+284insCGG	ENSP00000482149.2:n.*139+283_*139+284insCGG
ENST00000683378.1:n.245+283_245+284insCGG
ENST00000345378.7:c.1022+283_1022+284insCGG	ENSP00000223366.2:n.1022+283_1022+284insCGG
ENST00000403799.8:c.1019+283_1019+284insCGG MANE Select	ENSP00000384247.3:n.1019+283_1019+284insCGG
ENST00000671824.1:c.1082+283_1082+284insCGG	ENSP00000500264.1:n.1082+283_1082+284insCGG
ENST00000673284.1:c.1019+283_1019+284insCGG	ENSP00000499852.1:n.1019+283_1019+284insCGG
ENST00000345378.6:c.1022+283_1022+284insCGG	ENSP00000223366.2:n.1022+283_1022+284insCGG
ENST00000395796.7:c.1016+283_1016+284insCGG	ENSP00000379142.3:n.1016+283_1016+284insCGG
ENST00000403799.7:c.1019+283_1019+284insCGG	ENSP00000384247.3:n.1019+283_1019+284insCGG
ENST00000437084.1:c.968+283_968+284insCGG	ENSP00000402840.1:n.968+283_968+284insCGG
ENST00000473353.1:n.317+283_317+284insCGG
ENST00000616242.4:c.1016+283_1016+284insCGG	ENSP00000482149.1:n.1016+283_1016+284insCGG
NM_000162.3:c.1019+283_1019+284insCGG	NP_000153.1:n.1019+283_1019+284insCGG
NM_033507.1:c.1022+283_1022+284insCGG	NP_277042.1:n.1022+283_1022+284insCGG
NM_033508.1:c.1016+283_1016+284insCGG	NP_277043.1:n.1016+283_1016+284insCGG
NM_000162.4:c.1019+283_1019+284insCGG	NP_000153.1:n.1019+283_1019+284insCGG
NM_001354800.1:c.1019+283_1019+284insCGG	NP_001341729.1:n.1019+283_1019+284insCGG
NM_001354801.1:c.8+439_8+440insCGG	NP_001341730.1:n.8+439_8+440insCGG
NM_033507.2:c.1022+283_1022+284insCGG	NP_277042.1:n.1022+283_1022+284insCGG
NM_033508.2:c.1016+283_1016+284insCGG	NP_277043.1:n.1016+283_1016+284insCGG
NM_000162.5:c.1019+283_1019+284insCGG MANE Select	NP_000153.1:n.1019+283_1019+284insCGG
NM_033507.3:c.1022+283_1022+284insCGG	NP_277042.1:n.1022+283_1022+284insCGG
NM_033508.3:c.1016+283_1016+284insCGG	NP_277043.1:n.1016+283_1016+284insCGG