Canonical Allele Identifier: CA454863055
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44185269C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145670C>G , CM000669.2:g.44145670C>G GRCh38
NC_000007.13:g.44185269C>G , CM000669.1:g.44185269C>G GRCh37
NC_000007.12:g.44151794C>G NCBI36
NG_008847.1:g.48754G>C
NG_008847.2:g.57501G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1078G>C ENSP00000379142.4:n.*1078G>C
ENST00000616242.5:c.*200G>C ENSP00000482149.2:n.*200G>C
ENST00000683378.1:n.306G>C
ENST00000336642.9:c.114G>C ENSP00000338009.5:p.Ser38=
ENST00000345378.7:c.1083G>C ENSP00000223366.2:p.Ser361=
ENST00000403799.8:c.1080G>C MANE Select ENSP00000384247.3:p.Ser360=
ENST00000671824.1:c.1143G>C ENSP00000500264.1:p.Ser381=
ENST00000672743.1:n.92G>C
ENST00000673284.1:c.1080G>C ENSP00000499852.1:p.Ser360=
ENST00000336642.8:c.132G>C ENSP00000338009.4:p.Ser44=
ENST00000345378.6:c.1083G>C ENSP00000223366.2:p.Ser361=
ENST00000395796.7:c.1077G>C ENSP00000379142.3:p.Ser359=
ENST00000403799.7:c.1080G>C ENSP00000384247.3:p.Ser360=
ENST00000437084.1:c.1029G>C ENSP00000402840.1:p.Ser343=
ENST00000459642.1:n.460G>C
ENST00000473353.1:n.378G>C
ENST00000616242.4:c.1077G>C ENSP00000482149.1:p.Ser359=
NM_000162.3:c.1080G>C NP_000153.1:p.Ser360=
NM_033507.1:c.1083G>C NP_277042.1:p.Ser361=
NM_033508.1:c.1077G>C NP_277043.1:p.Ser359=
NM_000162.4:c.1080G>C NP_000153.1:p.Ser360=
NM_001354800.1:c.1080G>C NP_001341729.1:p.Ser360=
NM_001354801.1:c.69G>C NP_001341730.1:p.Ser23=
NM_001354802.1:c.-61G>C NP_001341731.1:n.-61G>C
NM_001354803.1:c.114G>C NP_001341732.1:p.Ser38=
NM_033507.2:c.1083G>C NP_277042.1:p.Ser361=
NM_033508.2:c.1077G>C NP_277043.1:p.Ser359=
XM_024446707.1:c.-61G>C XP_024302475.1:n.-61G>C
NM_000162.5:c.1080G>C MANE Select NP_000153.1:p.Ser360=
NM_033507.3:c.1083G>C NP_277042.1:p.Ser361=
NM_033508.3:c.1077G>C NP_277043.1:p.Ser359=
NM_001354803.2:c.114G>C NP_001341732.1:p.Ser38=