Canonical Allele Identifier: CA1703637035
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44152292G= , CM000669.2:g.44152292G= GRCh38
NC_000007.13:g.44191891G= , CM000669.1:g.44191891G= GRCh37
NC_000007.12:g.44158416G= NCBI36
NG_008847.1:g.42132C=
NG_008847.2:g.50879C=

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*340C= ENSP00000379142.4:n.*340C=
ENST00000616242.5:c.342C= ENSP00000482149.2:p.Ala114=
ENST00000682635.1:n.828C=
ENST00000345378.7:c.345C= ENSP00000223366.2:p.Ala115=
ENST00000403799.8:c.342C= MANE Select ENSP00000384247.3:p.Ala114=
ENST00000671824.1:c.342C= ENSP00000500264.1:p.Ala114=
ENST00000673284.1:c.342C= ENSP00000499852.1:p.Ala114=
ENST00000345378.6:c.345C= ENSP00000223366.2:p.Ala115=
ENST00000395796.7:c.339C= ENSP00000379142.3:p.Ala113=
ENST00000403799.7:c.342C= ENSP00000384247.3:p.Ala114=
ENST00000437084.1:c.342C= ENSP00000402840.1:p.Ala114=
ENST00000616242.4:c.339C= ENSP00000482149.1:p.Ala113=
NM_000162.3:c.342C= NP_000153.1:p.Ala114=
NM_033507.1:c.345C= NP_277042.1:p.Ala115=
NM_033508.1:c.339C= NP_277043.1:p.Ala113=
NM_000162.4:c.342C= NP_000153.1:p.Ala114=
NM_001354800.1:c.342C= NP_001341729.1:p.Ala114=
NM_033507.2:c.345C= NP_277042.1:p.Ala115=
NM_033508.2:c.339C= NP_277043.1:p.Ala113=
NM_000162.5:c.342C= MANE Select NP_000153.1:p.Ala114=
NM_033507.3:c.345C= NP_277042.1:p.Ala115=
NM_033508.3:c.339C= NP_277043.1:p.Ala113=