Canonical Allele Identifier: CA1703612972
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145725G= , CM000669.2:g.44145725G= GRCh38
NC_000007.13:g.44185324G= , CM000669.1:g.44185324G= GRCh37
NC_000007.12:g.44151849G= NCBI36
NG_008847.1:g.48699C=
NG_008847.2:g.57446C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1023C= ENSP00000379142.4:n.*1023C=
ENST00000616242.5:c.*145C= ENSP00000482149.2:n.*145C=
ENST00000683378.1:n.251C=
ENST00000336642.9:c.59C= ENSP00000338009.5:p.Thr20=
ENST00000345378.7:c.1028C= ENSP00000223366.2:p.Thr343=
ENST00000403799.8:c.1025C= MANE Select ENSP00000384247.3:p.Thr342=
ENST00000671824.1:c.1088C= ENSP00000500264.1:p.Thr363=
ENST00000672743.1:n.37C=
ENST00000673284.1:c.1025C= ENSP00000499852.1:p.Thr342=
ENST00000336642.8:c.77C= ENSP00000338009.4:p.Thr26=
ENST00000345378.6:c.1028C= ENSP00000223366.2:p.Thr343=
ENST00000395796.7:c.1022C= ENSP00000379142.3:p.Thr341=
ENST00000403799.7:c.1025C= ENSP00000384247.3:p.Thr342=
ENST00000437084.1:c.974C= ENSP00000402840.1:p.Thr325=
ENST00000459642.1:n.405C=
ENST00000473353.1:n.323C=
ENST00000616242.4:c.1022C= ENSP00000482149.1:p.Thr341=
NM_000162.3:c.1025C= NP_000153.1:p.Thr342=
NM_033507.1:c.1028C= NP_277042.1:p.Thr343=
NM_033508.1:c.1022C= NP_277043.1:p.Thr341=
NM_000162.4:c.1025C= NP_000153.1:p.Thr342=
NM_001354800.1:c.1025C= NP_001341729.1:p.Thr342=
NM_001354801.1:c.14C= NP_001341730.1:p.Thr5=
NM_001354802.1:c.-116C= NP_001341731.1:n.-116C=
NM_001354803.1:c.59C= NP_001341732.1:p.Thr20=
NM_033507.2:c.1028C= NP_277042.1:p.Thr343=
NM_033508.2:c.1022C= NP_277043.1:p.Thr341=
XM_024446707.1:c.-116C= XP_024302475.1:n.-116C=
NM_000162.5:c.1025C= MANE Select NP_000153.1:p.Thr342=
NM_033507.3:c.1028C= NP_277042.1:p.Thr343=
NM_033508.3:c.1022C= NP_277043.1:p.Thr341=
NM_001354803.2:c.59C= NP_001341732.1:p.Thr20=