Canonical Allele Identifier: CA2682585010

Gene: GCK

Linked Data

• gnomAD v4: 7-44146283-C-CCA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146283_44146284insCA , CM000669.2:g.44146283_44146284insCA	GRCh38
NC_000007.13:g.44185882_44185883insCA , CM000669.1:g.44185882_44185883insCA	GRCh37
NC_000007.12:g.44152407_44152408insCA	NCBI36
NG_008847.1:g.48140_48141insTG
NG_008847.2:g.56887_56888insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1017+179_*1017+180insTG	ENSP00000379142.4:n.*1017+179_*1017+180insTG
ENST00000616242.5:c.*139+179_*139+180insTG	ENSP00000482149.2:n.*139+179_*139+180insTG
ENST00000683378.1:n.245+179_245+180insTG
ENST00000345378.7:c.1022+179_1022+180insTG	ENSP00000223366.2:n.1022+179_1022+180insTG
ENST00000403799.8:c.1019+179_1019+180insTG MANE Select	ENSP00000384247.3:n.1019+179_1019+180insTG
ENST00000671824.1:c.1082+179_1082+180insTG	ENSP00000500264.1:n.1082+179_1082+180insTG
ENST00000673284.1:c.1019+179_1019+180insTG	ENSP00000499852.1:n.1019+179_1019+180insTG
ENST00000345378.6:c.1022+179_1022+180insTG	ENSP00000223366.2:n.1022+179_1022+180insTG
ENST00000395796.7:c.1016+179_1016+180insTG	ENSP00000379142.3:n.1016+179_1016+180insTG
ENST00000403799.7:c.1019+179_1019+180insTG	ENSP00000384247.3:n.1019+179_1019+180insTG
ENST00000437084.1:c.968+179_968+180insTG	ENSP00000402840.1:n.968+179_968+180insTG
ENST00000473353.1:n.317+179_317+180insTG
ENST00000616242.4:c.1016+179_1016+180insTG	ENSP00000482149.1:n.1016+179_1016+180insTG
NM_000162.3:c.1019+179_1019+180insTG	NP_000153.1:n.1019+179_1019+180insTG
NM_033507.1:c.1022+179_1022+180insTG	NP_277042.1:n.1022+179_1022+180insTG
NM_033508.1:c.1016+179_1016+180insTG	NP_277043.1:n.1016+179_1016+180insTG
NM_000162.4:c.1019+179_1019+180insTG	NP_000153.1:n.1019+179_1019+180insTG
NM_001354800.1:c.1019+179_1019+180insTG	NP_001341729.1:n.1019+179_1019+180insTG
NM_001354801.1:c.8+335_8+336insTG	NP_001341730.1:n.8+335_8+336insTG
NM_033507.2:c.1022+179_1022+180insTG	NP_277042.1:n.1022+179_1022+180insTG
NM_033508.2:c.1016+179_1016+180insTG	NP_277043.1:n.1016+179_1016+180insTG
NM_000162.5:c.1019+179_1019+180insTG MANE Select	NP_000153.1:n.1019+179_1019+180insTG
NM_033507.3:c.1022+179_1022+180insTG	NP_277042.1:n.1022+179_1022+180insTG
NM_033508.3:c.1016+179_1016+180insTG	NP_277043.1:n.1016+179_1016+180insTG