Canonical Allele Identifier: CA454607900

Gene: GCK

Linked Data

• gnomAD v4: 7-44146558-C-T
• MyVariant Identifiers: chr7:g.44186157C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146558C>T , CM000669.2:g.44146558C>T	GRCh38
NC_000007.13:g.44186157C>T , CM000669.1:g.44186157C>T	GRCh37
NC_000007.12:g.44152682C>T	NCBI36
NG_008847.1:g.47866G>A
NG_008847.2:g.56613G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*922G>A	ENSP00000379142.4:n.*922G>A
ENST00000616242.5:c.*44G>A	ENSP00000482149.2:n.*44G>A
ENST00000683378.1:n.150G>A
ENST00000345378.7:c.927G>A	ENSP00000223366.2:p.Arg309=
ENST00000403799.8:c.924G>A MANE Select	ENSP00000384247.3:p.Arg308=
ENST00000671824.1:c.987G>A	ENSP00000500264.1:p.Arg329=
ENST00000673284.1:c.924G>A	ENSP00000499852.1:p.Arg308=
ENST00000345378.6:c.927G>A	ENSP00000223366.2:p.Arg309=
ENST00000395796.7:c.921G>A	ENSP00000379142.3:p.Arg307=
ENST00000403799.7:c.924G>A	ENSP00000384247.3:p.Arg308=
ENST00000437084.1:c.873G>A	ENSP00000402840.1:p.Arg291=
ENST00000473353.1:n.222G>A
ENST00000616242.4:c.921G>A	ENSP00000482149.1:p.Arg307=
NM_000162.3:c.924G>A	NP_000153.1:p.Arg308=
NM_033507.1:c.927G>A	NP_277042.1:p.Arg309=
NM_033508.1:c.921G>A	NP_277043.1:p.Arg307=
NM_000162.4:c.924G>A	NP_000153.1:p.Arg308=
NM_001354800.1:c.924G>A	NP_001341729.1:p.Arg308=
NM_001354801.1:c.8+61G>A	NP_001341730.1:n.8+61G>A
NM_033507.2:c.927G>A	NP_277042.1:p.Arg309=
NM_033508.2:c.921G>A	NP_277043.1:p.Arg307=
NM_000162.5:c.924G>A MANE Select	NP_000153.1:p.Arg308=
NM_033507.3:c.927G>A	NP_277042.1:p.Arg309=
NM_033508.3:c.921G>A	NP_277043.1:p.Arg307=