Canonical Allele Identifier: CA367400013

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44186158C>A (hg19) ; chr7:g.44146559C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146559C>A , CM000669.2:g.44146559C>A	GRCh38
NC_000007.13:g.44186158C>A , CM000669.1:g.44186158C>A	GRCh37
NC_000007.12:g.44152683C>A	NCBI36
NG_008847.1:g.47865G>T
NG_008847.2:g.56612G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*921G>T	ENSP00000379142.4:n.*921G>T
ENST00000616242.5:c.*43G>T	ENSP00000482149.2:n.*43G>T
ENST00000683378.1:n.149G>T
ENST00000345378.7:c.926G>T	ENSP00000223366.2:p.Arg309Met
ENST00000403799.8:c.923G>T MANE Select	ENSP00000384247.3:p.Arg308Met
ENST00000671824.1:c.986G>T	ENSP00000500264.1:p.Arg329Met
ENST00000673284.1:c.923G>T	ENSP00000499852.1:p.Arg308Met
ENST00000345378.6:c.926G>T	ENSP00000223366.2:p.Arg309Met
ENST00000395796.7:c.920G>T	ENSP00000379142.3:p.Arg307Met
ENST00000403799.7:c.923G>T	ENSP00000384247.3:p.Arg308Met
ENST00000437084.1:c.872G>T	ENSP00000402840.1:p.Arg291Met
ENST00000473353.1:n.221G>T
ENST00000616242.4:c.920G>T	ENSP00000482149.1:p.Arg307Met
NM_000162.3:c.923G>T	NP_000153.1:p.Arg308Met
NM_033507.1:c.926G>T	NP_277042.1:p.Arg309Met
NM_033508.1:c.920G>T	NP_277043.1:p.Arg307Met
NM_000162.4:c.923G>T	NP_000153.1:p.Arg308Met
NM_001354800.1:c.923G>T	NP_001341729.1:p.Arg308Met
NM_001354801.1:c.8+60G>T	NP_001341730.1:n.8+60G>T
NM_033507.2:c.926G>T	NP_277042.1:p.Arg309Met
NM_033508.2:c.920G>T	NP_277043.1:p.Arg307Met
NM_000162.5:c.923G>T MANE Select	NP_000153.1:p.Arg308Met
NM_033507.3:c.926G>T	NP_277042.1:p.Arg309Met
NM_033508.3:c.920G>T	NP_277043.1:p.Arg307Met