Canonical Allele Identifier: CA1703612934
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145637G= , CM000669.2:g.44145637G= GRCh38
NC_000007.13:g.44185236G= , CM000669.1:g.44185236G= GRCh37
NC_000007.12:g.44151761G= NCBI36
NG_008847.1:g.48787C=
NG_008847.2:g.57534C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1111C= ENSP00000379142.4:n.*1111C=
ENST00000616242.5:c.*233C= ENSP00000482149.2:n.*233C=
ENST00000683378.1:n.339C=
ENST00000336642.9:c.147C= ENSP00000338009.5:p.Cys49=
ENST00000345378.7:c.1116C= ENSP00000223366.2:p.Cys372=
ENST00000403799.8:c.1113C= MANE Select ENSP00000384247.3:p.Cys371=
ENST00000671824.1:c.1176C= ENSP00000500264.1:p.Cys392=
ENST00000672743.1:n.125C=
ENST00000673284.1:c.1113C= ENSP00000499852.1:p.Cys371=
ENST00000336642.8:c.165C= ENSP00000338009.4:p.Cys55=
ENST00000345378.6:c.1116C= ENSP00000223366.2:p.Cys372=
ENST00000395796.7:c.1110C= ENSP00000379142.3:p.Cys370=
ENST00000403799.7:c.1113C= ENSP00000384247.3:p.Cys371=
ENST00000437084.1:c.1062C= ENSP00000402840.1:p.Cys354=
ENST00000459642.1:n.493C=
ENST00000616242.4:c.1110C= ENSP00000482149.1:p.Cys370=
NM_000162.3:c.1113C= NP_000153.1:p.Cys371=
NM_033507.1:c.1116C= NP_277042.1:p.Cys372=
NM_033508.1:c.1110C= NP_277043.1:p.Cys370=
NM_000162.4:c.1113C= NP_000153.1:p.Cys371=
NM_001354800.1:c.1113C= NP_001341729.1:p.Cys371=
NM_001354801.1:c.102C= NP_001341730.1:p.Cys34=
NM_001354802.1:c.-28C= NP_001341731.1:n.-28C=
NM_001354803.1:c.147C= NP_001341732.1:p.Cys49=
NM_033507.2:c.1116C= NP_277042.1:p.Cys372=
NM_033508.2:c.1110C= NP_277043.1:p.Cys370=
XM_024446707.1:c.-28C= XP_024302475.1:n.-28C=
NM_000162.5:c.1113C= MANE Select NP_000153.1:p.Cys371=
NM_033507.3:c.1116C= NP_277042.1:p.Cys372=
NM_033508.3:c.1110C= NP_277043.1:p.Cys370=
NM_001354803.2:c.147C= NP_001341732.1:p.Cys49=