Canonical Allele Identifier: CA454608970
Gene: GCK HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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