Canonical Allele Identifier: CA454607379

Gene: GCK

Linked Data

• gnomAD v4: 7-44146272-C-CG
• MyVariant Identifiers: chr7:g.44185871_44185872insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146275dup , CM000669.2:g.44146275dup	GRCh38
NC_000007.13:g.44185874dup , CM000669.1:g.44185874dup	GRCh37
NC_000007.12:g.44152399dup	NCBI36
NG_008847.1:g.48151dup
NG_008847.2:g.56898dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1017+190dup	ENSP00000379142.4:n.*1017+190dup
ENST00000616242.5:c.*139+190dup	ENSP00000482149.2:n.*139+190dup
ENST00000683378.1:n.245+190dup
ENST00000345378.7:c.1022+190dup	ENSP00000223366.2:n.1022+190dup
ENST00000403799.8:c.1019+190dup MANE Select	ENSP00000384247.3:n.1019+190dup
ENST00000671824.1:c.1082+190dup	ENSP00000500264.1:n.1082+190dup
ENST00000673284.1:c.1019+190dup	ENSP00000499852.1:n.1019+190dup
ENST00000345378.6:c.1022+190dup	ENSP00000223366.2:n.1022+190dup
ENST00000395796.7:c.1016+190dup	ENSP00000379142.3:n.1016+190dup
ENST00000403799.7:c.1019+190dup	ENSP00000384247.3:n.1019+190dup
ENST00000437084.1:c.968+190dup	ENSP00000402840.1:n.968+190dup
ENST00000473353.1:n.317+190dup
ENST00000616242.4:c.1016+190dup	ENSP00000482149.1:n.1016+190dup
NM_000162.3:c.1019+190dup	NP_000153.1:n.1019+190dup
NM_033507.1:c.1022+190dup	NP_277042.1:n.1022+190dup
NM_033508.1:c.1016+190dup	NP_277043.1:n.1016+190dup
NM_000162.4:c.1019+190dup	NP_000153.1:n.1019+190dup
NM_001354800.1:c.1019+190dup	NP_001341729.1:n.1019+190dup
NM_001354801.1:c.8+346dup	NP_001341730.1:n.8+346dup
NM_033507.2:c.1022+190dup	NP_277042.1:n.1022+190dup
NM_033508.2:c.1016+190dup	NP_277043.1:n.1016+190dup
NM_000162.5:c.1019+190dup MANE Select	NP_000153.1:n.1019+190dup
NM_033507.3:c.1022+190dup	NP_277042.1:n.1022+190dup
NM_033508.3:c.1016+190dup	NP_277043.1:n.1016+190dup