Canonical Allele Identifier: CA1703612953
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145679C= , CM000669.2:g.44145679C= GRCh38
NC_000007.13:g.44185278C= , CM000669.1:g.44185278C= GRCh37
NC_000007.12:g.44151803C= NCBI36
NG_008847.1:g.48745G=
NG_008847.2:g.57492G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1069G= ENSP00000379142.4:n.*1069G=
ENST00000616242.5:c.*191G= ENSP00000482149.2:n.*191G=
ENST00000683378.1:n.297G=
ENST00000336642.9:c.105G= ENSP00000338009.5:p.Leu35=
ENST00000345378.7:c.1074G= ENSP00000223366.2:p.Leu358=
ENST00000403799.8:c.1071G= MANE Select ENSP00000384247.3:p.Leu357=
ENST00000671824.1:c.1134G= ENSP00000500264.1:p.Leu378=
ENST00000672743.1:n.83G=
ENST00000673284.1:c.1071G= ENSP00000499852.1:p.Leu357=
ENST00000336642.8:c.123G= ENSP00000338009.4:p.Leu41=
ENST00000345378.6:c.1074G= ENSP00000223366.2:p.Leu358=
ENST00000395796.7:c.1068G= ENSP00000379142.3:p.Leu356=
ENST00000403799.7:c.1071G= ENSP00000384247.3:p.Leu357=
ENST00000437084.1:c.1020G= ENSP00000402840.1:p.Leu340=
ENST00000459642.1:n.451G=
ENST00000473353.1:n.369G=
ENST00000616242.4:c.1068G= ENSP00000482149.1:p.Leu356=
NM_000162.3:c.1071G= NP_000153.1:p.Leu357=
NM_033507.1:c.1074G= NP_277042.1:p.Leu358=
NM_033508.1:c.1068G= NP_277043.1:p.Leu356=
NM_000162.4:c.1071G= NP_000153.1:p.Leu357=
NM_001354800.1:c.1071G= NP_001341729.1:p.Leu357=
NM_001354801.1:c.60G= NP_001341730.1:p.Leu20=
NM_001354802.1:c.-70G= NP_001341731.1:n.-70G=
NM_001354803.1:c.105G= NP_001341732.1:p.Leu35=
NM_033507.2:c.1074G= NP_277042.1:p.Leu358=
NM_033508.2:c.1068G= NP_277043.1:p.Leu356=
XM_024446707.1:c.-70G= XP_024302475.1:n.-70G=
NM_000162.5:c.1071G= MANE Select NP_000153.1:p.Leu357=
NM_033507.3:c.1074G= NP_277042.1:p.Leu358=
NM_033508.3:c.1068G= NP_277043.1:p.Leu356=
NM_001354803.2:c.105G= NP_001341732.1:p.Leu35=