Canonical Allele Identifier: CA367397013

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44184809C>G (hg19) ; chr7:g.44145210C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145210C>G , CM000669.2:g.44145210C>G	GRCh38
NC_000007.13:g.44184809C>G , CM000669.1:g.44184809C>G	GRCh37
NC_000007.12:g.44151334C>G	NCBI36
NG_008847.1:g.49214G>C
NG_008847.2:g.57961G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1322G>C	ENSP00000379142.4:n.*1322G>C
ENST00000616242.5:c.*444G>C	ENSP00000482149.2:n.*444G>C
ENST00000683378.1:n.550G>C
ENST00000336642.9:c.358G>C	ENSP00000338009.5:p.Glu120Gln
ENST00000345378.7:c.1327G>C	ENSP00000223366.2:p.Glu443Gln
ENST00000403799.8:c.1324G>C MANE Select	ENSP00000384247.3:p.Glu442Gln
ENST00000671824.1:c.1387G>C	ENSP00000500264.1:p.Glu463Gln
ENST00000672743.1:n.336G>C
ENST00000673284.1:c.1324G>C	ENSP00000499852.1:p.Glu442Gln
ENST00000336642.8:c.376G>C	ENSP00000338009.4:p.Glu126Gln
ENST00000345378.6:c.1327G>C	ENSP00000223366.2:p.Glu443Gln
ENST00000395796.7:c.1321G>C	ENSP00000379142.3:p.Glu441Gln
ENST00000403799.7:c.1324G>C	ENSP00000384247.3:p.Glu442Gln
ENST00000437084.1:c.1273G>C	ENSP00000402840.1:p.Glu425Gln
ENST00000459642.1:n.704G>C
ENST00000616242.4:c.1321G>C	ENSP00000482149.1:p.Glu441Gln
NM_000162.3:c.1324G>C	NP_000153.1:p.Glu442Gln
NM_033507.1:c.1327G>C	NP_277042.1:p.Glu443Gln
NM_033508.1:c.1321G>C	NP_277043.1:p.Glu441Gln
NM_000162.4:c.1324G>C	NP_000153.1:p.Glu442Gln
NM_001354800.1:c.1324G>C	NP_001341729.1:p.Glu442Gln
NM_001354801.1:c.313G>C	NP_001341730.1:p.Glu105Gln
NM_001354802.1:c.184G>C	NP_001341731.1:p.Glu62Gln
NM_001354803.1:c.358G>C	NP_001341732.1:p.Glu120Gln
NM_033507.2:c.1327G>C	NP_277042.1:p.Glu443Gln
NM_033508.2:c.1321G>C	NP_277043.1:p.Glu441Gln
XM_024446707.1:c.184G>C	XP_024302475.1:p.Glu62Gln
NM_000162.5:c.1324G>C MANE Select	NP_000153.1:p.Glu442Gln
NM_033507.3:c.1327G>C	NP_277042.1:p.Glu443Gln
NM_033508.3:c.1321G>C	NP_277043.1:p.Glu441Gln
NM_001354803.2:c.358G>C	NP_001341732.1:p.Glu120Gln