Canonical Allele Identifier: CA367403739

Gene: GCK

Linked Data

• COSMIC: COSM746804 ; COSM746805 ; COSM4859920
• MyVariant Identifiers: chr7:g.44193036C>A (hg19) ; chr7:g.44153437C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153437C>A , CM000669.2:g.44153437C>A	GRCh38
NC_000007.13:g.44193036C>A , CM000669.1:g.44193036C>A	GRCh37
NC_000007.12:g.44159561C>A	NCBI36
NG_008847.1:g.40987G>T
NG_008847.2:g.49734G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*70G>T	ENSP00000379142.4:n.*70G>T
ENST00000616242.5:c.72G>T	ENSP00000482149.2:p.Gln24His
ENST00000682635.1:n.558G>T
ENST00000345378.7:c.75G>T	ENSP00000223366.2:p.Gln25His
ENST00000403799.8:c.72G>T MANE Select	ENSP00000384247.3:p.Gln24His
ENST00000671824.1:c.72G>T	ENSP00000500264.1:p.Gln24His
ENST00000673284.1:c.72G>T	ENSP00000499852.1:p.Gln24His
ENST00000345378.6:c.75G>T	ENSP00000223366.2:p.Gln25His
ENST00000395796.7:c.69G>T	ENSP00000379142.3:p.Gln23His
ENST00000403799.7:c.72G>T	ENSP00000384247.3:p.Gln24His
ENST00000437084.1:c.72G>T	ENSP00000402840.1:p.Gln24His
ENST00000476008.1:n.507G>T
ENST00000616242.4:c.69G>T	ENSP00000482149.1:p.Gln23His
NM_000162.3:c.72G>T	NP_000153.1:p.Gln24His
NM_033507.1:c.75G>T	NP_277042.1:p.Gln25His
NM_033508.1:c.69G>T	NP_277043.1:p.Gln23His
NM_000162.4:c.72G>T	NP_000153.1:p.Gln24His
NM_001354800.1:c.72G>T	NP_001341729.1:p.Gln24His
NM_033507.2:c.75G>T	NP_277042.1:p.Gln25His
NM_033508.2:c.69G>T	NP_277043.1:p.Gln23His
NM_000162.5:c.72G>T MANE Select	NP_000153.1:p.Gln24His
NM_033507.3:c.75G>T	NP_277042.1:p.Gln25His
NM_033508.3:c.69G>T	NP_277043.1:p.Gln23His