Canonical Allele Identifier: CA454609024

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44189390T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149791T>C , CM000669.2:g.44149791T>C	GRCh38
NC_000007.13:g.44189390T>C , CM000669.1:g.44189390T>C	GRCh37
NC_000007.12:g.44155915T>C	NCBI36
NG_008847.1:g.44633A>G
NG_008847.2:g.53380A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*646A>G	ENSP00000379142.4:n.*646A>G
ENST00000616242.5:c.648A>G	ENSP00000482149.2:p.Glu216=
ENST00000682635.1:n.1134A>G
ENST00000345378.7:c.651A>G	ENSP00000223366.2:p.Glu217=
ENST00000403799.8:c.648A>G MANE Select	ENSP00000384247.3:p.Glu216=
ENST00000671824.1:c.648A>G	ENSP00000500264.1:p.Glu216=
ENST00000673284.1:c.648A>G	ENSP00000499852.1:p.Glu216=
ENST00000345378.6:c.651A>G	ENSP00000223366.2:p.Glu217=
ENST00000395796.7:c.645A>G	ENSP00000379142.3:p.Glu215=
ENST00000403799.7:c.648A>G	ENSP00000384247.3:p.Glu216=
ENST00000437084.1:c.597A>G	ENSP00000402840.1:p.Glu199=
ENST00000616242.4:c.645A>G	ENSP00000482149.1:p.Glu215=
NM_000162.3:c.648A>G	NP_000153.1:p.Glu216=
NM_033507.1:c.651A>G	NP_277042.1:p.Glu217=
NM_033508.1:c.645A>G	NP_277043.1:p.Glu215=
NM_000162.4:c.648A>G	NP_000153.1:p.Glu216=
NM_001354800.1:c.648A>G	NP_001341729.1:p.Glu216=
NM_033507.2:c.651A>G	NP_277042.1:p.Glu217=
NM_033508.2:c.645A>G	NP_277043.1:p.Glu215=
NM_000162.5:c.648A>G MANE Select	NP_000153.1:p.Glu216=
NM_033507.3:c.651A>G	NP_277042.1:p.Glu217=
NM_033508.3:c.645A>G	NP_277043.1:p.Glu215=