Canonical Allele Identifier: CA454608969

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44189369G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149770G>T , CM000669.2:g.44149770G>T	GRCh38
NC_000007.13:g.44189369G>T , CM000669.1:g.44189369G>T	GRCh37
NC_000007.12:g.44155894G>T	NCBI36
NG_008847.1:g.44654C>A
NG_008847.2:g.53401C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*667C>A	ENSP00000379142.4:n.*667C>A
ENST00000616242.5:c.669C>A	ENSP00000482149.2:p.Gly223=
ENST00000682635.1:n.1155C>A
ENST00000345378.7:c.672C>A	ENSP00000223366.2:p.Gly224=
ENST00000403799.8:c.669C>A MANE Select	ENSP00000384247.3:p.Gly223=
ENST00000671824.1:c.669C>A	ENSP00000500264.1:p.Gly223=
ENST00000673284.1:c.669C>A	ENSP00000499852.1:p.Gly223=
ENST00000345378.6:c.672C>A	ENSP00000223366.2:p.Gly224=
ENST00000395796.7:c.666C>A	ENSP00000379142.3:p.Gly222=
ENST00000403799.7:c.669C>A	ENSP00000384247.3:p.Gly223=
ENST00000437084.1:c.618C>A	ENSP00000402840.1:p.Gly206=
ENST00000616242.4:c.666C>A	ENSP00000482149.1:p.Gly222=
NM_000162.3:c.669C>A	NP_000153.1:p.Gly223=
NM_033507.1:c.672C>A	NP_277042.1:p.Gly224=
NM_033508.1:c.666C>A	NP_277043.1:p.Gly222=
XR_927223.1:n.285G>T
NM_000162.4:c.669C>A	NP_000153.1:p.Gly223=
NM_001354800.1:c.669C>A	NP_001341729.1:p.Gly223=
NM_033507.2:c.672C>A	NP_277042.1:p.Gly224=
NM_033508.2:c.666C>A	NP_277043.1:p.Gly222=
XR_927223.2:n.285G>T
NM_000162.5:c.669C>A MANE Select	NP_000153.1:p.Gly223=
NM_033507.3:c.672C>A	NP_277042.1:p.Gly224=
NM_033508.3:c.666C>A	NP_277043.1:p.Gly222=