Canonical Allele Identifier: CA2682585144

Gene: GCK

Linked Data

• gnomAD v4: 7-44146291-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146291_44146292insA , CM000669.2:g.44146291_44146292insA	GRCh38
NC_000007.13:g.44185890_44185891insA , CM000669.1:g.44185890_44185891insA	GRCh37
NC_000007.12:g.44152415_44152416insA	NCBI36
NG_008847.1:g.48132_48133insT
NG_008847.2:g.56879_56880insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1017+171_*1017+172insT	ENSP00000379142.4:n.*1017+171_*1017+172insT
ENST00000616242.5:c.*139+171_*139+172insT	ENSP00000482149.2:n.*139+171_*139+172insT
ENST00000683378.1:n.245+171_245+172insT
ENST00000345378.7:c.1022+171_1022+172insT	ENSP00000223366.2:n.1022+171_1022+172insT
ENST00000403799.8:c.1019+171_1019+172insT MANE Select	ENSP00000384247.3:n.1019+171_1019+172insT
ENST00000671824.1:c.1082+171_1082+172insT	ENSP00000500264.1:n.1082+171_1082+172insT
ENST00000673284.1:c.1019+171_1019+172insT	ENSP00000499852.1:n.1019+171_1019+172insT
ENST00000345378.6:c.1022+171_1022+172insT	ENSP00000223366.2:n.1022+171_1022+172insT
ENST00000395796.7:c.1016+171_1016+172insT	ENSP00000379142.3:n.1016+171_1016+172insT
ENST00000403799.7:c.1019+171_1019+172insT	ENSP00000384247.3:n.1019+171_1019+172insT
ENST00000437084.1:c.968+171_968+172insT	ENSP00000402840.1:n.968+171_968+172insT
ENST00000473353.1:n.317+171_317+172insT
ENST00000616242.4:c.1016+171_1016+172insT	ENSP00000482149.1:n.1016+171_1016+172insT
NM_000162.3:c.1019+171_1019+172insT	NP_000153.1:n.1019+171_1019+172insT
NM_033507.1:c.1022+171_1022+172insT	NP_277042.1:n.1022+171_1022+172insT
NM_033508.1:c.1016+171_1016+172insT	NP_277043.1:n.1016+171_1016+172insT
NM_000162.4:c.1019+171_1019+172insT	NP_000153.1:n.1019+171_1019+172insT
NM_001354800.1:c.1019+171_1019+172insT	NP_001341729.1:n.1019+171_1019+172insT
NM_001354801.1:c.8+327_8+328insT	NP_001341730.1:n.8+327_8+328insT
NM_033507.2:c.1022+171_1022+172insT	NP_277042.1:n.1022+171_1022+172insT
NM_033508.2:c.1016+171_1016+172insT	NP_277043.1:n.1016+171_1016+172insT
NM_000162.5:c.1019+171_1019+172insT MANE Select	NP_000153.1:n.1019+171_1019+172insT
NM_033507.3:c.1022+171_1022+172insT	NP_277042.1:n.1022+171_1022+172insT
NM_033508.3:c.1016+171_1016+172insT	NP_277043.1:n.1016+171_1016+172insT