Canonical Allele Identifier: CA454607382

Gene: GCK

Linked Data

• dbSNP Id: rs1321551905
• gnomAD v2: 7-44185887-C-CA
• gnomAD v3: 7-44146288-C-CA
• gnomAD v4: 7-44146288-C-CA
• MyVariant Identifiers: chr7:g.44185887_44185888insA (hg19) ; chr7:g.44146288_44146289insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146288_44146289insA , CM000669.2:g.44146288_44146289insA	GRCh38
NC_000007.13:g.44185887_44185888insA , CM000669.1:g.44185887_44185888insA	GRCh37
NC_000007.12:g.44152412_44152413insA	NCBI36
NG_008847.1:g.48135_48136insT
NG_008847.2:g.56882_56883insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1017+174_*1017+175insT	ENSP00000379142.4:n.*1017+174_*1017+175insT
ENST00000616242.5:c.*139+174_*139+175insT	ENSP00000482149.2:n.*139+174_*139+175insT
ENST00000683378.1:n.245+174_245+175insT
ENST00000345378.7:c.1022+174_1022+175insT	ENSP00000223366.2:n.1022+174_1022+175insT
ENST00000403799.8:c.1019+174_1019+175insT MANE Select	ENSP00000384247.3:n.1019+174_1019+175insT
ENST00000671824.1:c.1082+174_1082+175insT	ENSP00000500264.1:n.1082+174_1082+175insT
ENST00000673284.1:c.1019+174_1019+175insT	ENSP00000499852.1:n.1019+174_1019+175insT
ENST00000345378.6:c.1022+174_1022+175insT	ENSP00000223366.2:n.1022+174_1022+175insT
ENST00000395796.7:c.1016+174_1016+175insT	ENSP00000379142.3:n.1016+174_1016+175insT
ENST00000403799.7:c.1019+174_1019+175insT	ENSP00000384247.3:n.1019+174_1019+175insT
ENST00000437084.1:c.968+174_968+175insT	ENSP00000402840.1:n.968+174_968+175insT
ENST00000473353.1:n.317+174_317+175insT
ENST00000616242.4:c.1016+174_1016+175insT	ENSP00000482149.1:n.1016+174_1016+175insT
NM_000162.3:c.1019+174_1019+175insT	NP_000153.1:n.1019+174_1019+175insT
NM_033507.1:c.1022+174_1022+175insT	NP_277042.1:n.1022+174_1022+175insT
NM_033508.1:c.1016+174_1016+175insT	NP_277043.1:n.1016+174_1016+175insT
NM_000162.4:c.1019+174_1019+175insT	NP_000153.1:n.1019+174_1019+175insT
NM_001354800.1:c.1019+174_1019+175insT	NP_001341729.1:n.1019+174_1019+175insT
NM_001354801.1:c.8+330_8+331insT	NP_001341730.1:n.8+330_8+331insT
NM_033507.2:c.1022+174_1022+175insT	NP_277042.1:n.1022+174_1022+175insT
NM_033508.2:c.1016+174_1016+175insT	NP_277043.1:n.1016+174_1016+175insT
NM_000162.5:c.1019+174_1019+175insT MANE Select	NP_000153.1:n.1019+174_1019+175insT
NM_033507.3:c.1022+174_1022+175insT	NP_277042.1:n.1022+174_1022+175insT
NM_033508.3:c.1016+174_1016+175insT	NP_277043.1:n.1016+174_1016+175insT