Canonical Allele Identifier: CA367396930

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44184790C>G (hg19) ; chr7:g.44145191C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145191C>G , CM000669.2:g.44145191C>G	GRCh38
NC_000007.13:g.44184790C>G , CM000669.1:g.44184790C>G	GRCh37
NC_000007.12:g.44151315C>G	NCBI36
NG_008847.1:g.49233G>C
NG_008847.2:g.57980G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1341G>C	ENSP00000379142.4:n.*1341G>C
ENST00000616242.5:c.*463G>C	ENSP00000482149.2:n.*463G>C
ENST00000683378.1:n.569G>C
ENST00000336642.9:c.377G>C	ENSP00000338009.5:p.Gly126Ala
ENST00000345378.7:c.1346G>C	ENSP00000223366.2:p.Gly449Ala
ENST00000403799.8:c.1343G>C MANE Select	ENSP00000384247.3:p.Gly448Ala
ENST00000671824.1:c.1406G>C	ENSP00000500264.1:p.Gly469Ala
ENST00000672743.1:n.355G>C
ENST00000673284.1:c.1343G>C	ENSP00000499852.1:p.Gly448Ala
ENST00000336642.8:c.395G>C	ENSP00000338009.4:p.Gly132Ala
ENST00000345378.6:c.1346G>C	ENSP00000223366.2:p.Gly449Ala
ENST00000395796.7:c.1340G>C	ENSP00000379142.3:p.Gly447Ala
ENST00000403799.7:c.1343G>C	ENSP00000384247.3:p.Gly448Ala
ENST00000437084.1:c.1292G>C	ENSP00000402840.1:p.Gly431Ala
ENST00000459642.1:n.723G>C
ENST00000616242.4:c.1340G>C	ENSP00000482149.1:p.Gly447Ala
NM_000162.3:c.1343G>C	NP_000153.1:p.Gly448Ala
NM_033507.1:c.1346G>C	NP_277042.1:p.Gly449Ala
NM_033508.1:c.1340G>C	NP_277043.1:p.Gly447Ala
NM_000162.4:c.1343G>C	NP_000153.1:p.Gly448Ala
NM_001354800.1:c.1343G>C	NP_001341729.1:p.Gly448Ala
NM_001354801.1:c.332G>C	NP_001341730.1:p.Gly111Ala
NM_001354802.1:c.203G>C	NP_001341731.1:p.Gly68Ala
NM_001354803.1:c.377G>C	NP_001341732.1:p.Gly126Ala
NM_033507.2:c.1346G>C	NP_277042.1:p.Gly449Ala
NM_033508.2:c.1340G>C	NP_277043.1:p.Gly447Ala
XM_024446707.1:c.203G>C	XP_024302475.1:p.Gly68Ala
NM_000162.5:c.1343G>C MANE Select	NP_000153.1:p.Gly448Ala
NM_033507.3:c.1346G>C	NP_277042.1:p.Gly449Ala
NM_033508.3:c.1340G>C	NP_277043.1:p.Gly447Ala
NM_001354803.2:c.377G>C	NP_001341732.1:p.Gly126Ala