Canonical Allele Identifier: CA1703612858
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145529G= , CM000669.2:g.44145529G= GRCh38
NC_000007.13:g.44185128G= , CM000669.1:g.44185128G= GRCh37
NC_000007.12:g.44151653G= NCBI36
NG_008847.1:g.48895C=
NG_008847.2:g.57642C=

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*1219C= ENSP00000379142.4:n.*1219C=
ENST00000616242.5:c.*341C= ENSP00000482149.2:n.*341C=
ENST00000683378.1:n.447C=
ENST00000336642.9:c.255C= ENSP00000338009.5:p.Gly85=
ENST00000345378.7:c.1224C= ENSP00000223366.2:p.Gly408=
ENST00000403799.8:c.1221C= MANE Select ENSP00000384247.3:p.Gly407=
ENST00000671824.1:c.1284C= ENSP00000500264.1:p.Gly428=
ENST00000672743.1:n.233C=
ENST00000673284.1:c.1221C= ENSP00000499852.1:p.Gly407=
ENST00000336642.8:c.273C= ENSP00000338009.4:p.Gly91=
ENST00000345378.6:c.1224C= ENSP00000223366.2:p.Gly408=
ENST00000395796.7:c.1218C= ENSP00000379142.3:p.Gly406=
ENST00000403799.7:c.1221C= ENSP00000384247.3:p.Gly407=
ENST00000437084.1:c.1170C= ENSP00000402840.1:p.Gly390=
ENST00000459642.1:n.601C=
ENST00000616242.4:c.1218C= ENSP00000482149.1:p.Gly406=
NM_000162.3:c.1221C= NP_000153.1:p.Gly407=
NM_033507.1:c.1224C= NP_277042.1:p.Gly408=
NM_033508.1:c.1218C= NP_277043.1:p.Gly406=
NM_000162.4:c.1221C= NP_000153.1:p.Gly407=
NM_001354800.1:c.1221C= NP_001341729.1:p.Gly407=
NM_001354801.1:c.210C= NP_001341730.1:p.Gly70=
NM_001354802.1:c.81C= NP_001341731.1:p.Gly27=
NM_001354803.1:c.255C= NP_001341732.1:p.Gly85=
NM_033507.2:c.1224C= NP_277042.1:p.Gly408=
NM_033508.2:c.1218C= NP_277043.1:p.Gly406=
XM_024446707.1:c.81C= XP_024302475.1:p.Gly27=
NM_000162.5:c.1221C= MANE Select NP_000153.1:p.Gly407=
NM_033507.3:c.1224C= NP_277042.1:p.Gly408=
NM_033508.3:c.1218C= NP_277043.1:p.Gly406=
NM_001354803.2:c.255C= NP_001341732.1:p.Gly85=