Canonical Allele Identifier: CA367396863

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44184772G>C (hg19) ; chr7:g.44145173G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145173G>C , CM000669.2:g.44145173G>C	GRCh38
NC_000007.13:g.44184772G>C , CM000669.1:g.44184772G>C	GRCh37
NC_000007.12:g.44151297G>C	NCBI36
NG_008847.1:g.49251C>G
NG_008847.2:g.57998C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*1359C>G	ENSP00000379142.4:n.*1359C>G
ENST00000616242.5:c.*481C>G	ENSP00000482149.2:n.*481C>G
ENST00000683378.1:n.587C>G
ENST00000336642.9:c.395C>G	ENSP00000338009.5:p.Ala132Gly
ENST00000345378.7:c.1364C>G	ENSP00000223366.2:p.Ala455Gly
ENST00000403799.8:c.1361C>G MANE Select	ENSP00000384247.3:p.Ala454Gly
ENST00000671824.1:c.1424C>G	ENSP00000500264.1:p.Ala475Gly
ENST00000672743.1:n.373C>G
ENST00000673284.1:c.1361C>G	ENSP00000499852.1:p.Ala454Gly
ENST00000336642.8:c.413C>G	ENSP00000338009.4:p.Ala138Gly
ENST00000345378.6:c.1364C>G	ENSP00000223366.2:p.Ala455Gly
ENST00000395796.7:c.1358C>G	ENSP00000379142.3:p.Ala453Gly
ENST00000403799.7:c.1361C>G	ENSP00000384247.3:p.Ala454Gly
ENST00000437084.1:c.1310C>G	ENSP00000402840.1:p.Ala437Gly
ENST00000459642.1:n.741C>G
ENST00000616242.4:c.1358C>G	ENSP00000482149.1:p.Ala453Gly
NM_000162.3:c.1361C>G	NP_000153.1:p.Ala454Gly
NM_033507.1:c.1364C>G	NP_277042.1:p.Ala455Gly
NM_033508.1:c.1358C>G	NP_277043.1:p.Ala453Gly
NM_000162.4:c.1361C>G	NP_000153.1:p.Ala454Gly
NM_001354800.1:c.1361C>G	NP_001341729.1:p.Ala454Gly
NM_001354801.1:c.350C>G	NP_001341730.1:p.Ala117Gly
NM_001354802.1:c.221C>G	NP_001341731.1:p.Ala74Gly
NM_001354803.1:c.395C>G	NP_001341732.1:p.Ala132Gly
NM_033507.2:c.1364C>G	NP_277042.1:p.Ala455Gly
NM_033508.2:c.1358C>G	NP_277043.1:p.Ala453Gly
XM_024446707.1:c.221C>G	XP_024302475.1:p.Ala74Gly
NM_000162.5:c.1361C>G MANE Select	NP_000153.1:p.Ala454Gly
NM_033507.3:c.1364C>G	NP_277042.1:p.Ala455Gly
NM_033508.3:c.1358C>G	NP_277043.1:p.Ala453Gly
NM_001354803.2:c.395C>G	NP_001341732.1:p.Ala132Gly