Canonical Allele Identifier: CA1703635856
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149773G= , CM000669.2:g.44149773G= GRCh38
NC_000007.13:g.44189372G= , CM000669.1:g.44189372G= GRCh37
NC_000007.12:g.44155897G= NCBI36
NG_008847.1:g.44651C=
NG_008847.2:g.53398C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*664C= ENSP00000379142.4:n.*664C=
ENST00000616242.5:c.666C= ENSP00000482149.2:p.Val222=
ENST00000682635.1:n.1152C=
ENST00000345378.7:c.669C= ENSP00000223366.2:p.Val223=
ENST00000403799.8:c.666C= MANE Select ENSP00000384247.3:p.Val222=
ENST00000671824.1:c.666C= ENSP00000500264.1:p.Val222=
ENST00000673284.1:c.666C= ENSP00000499852.1:p.Val222=
ENST00000345378.6:c.669C= ENSP00000223366.2:p.Val223=
ENST00000395796.7:c.663C= ENSP00000379142.3:p.Val221=
ENST00000403799.7:c.666C= ENSP00000384247.3:p.Val222=
ENST00000437084.1:c.615C= ENSP00000402840.1:p.Val205=
ENST00000616242.4:c.663C= ENSP00000482149.1:p.Val221=
NM_000162.3:c.666C= NP_000153.1:p.Val222=
NM_033507.1:c.669C= NP_277042.1:p.Val223=
NM_033508.1:c.663C= NP_277043.1:p.Val221=
XR_927223.1:n.288G=
NM_000162.4:c.666C= NP_000153.1:p.Val222=
NM_001354800.1:c.666C= NP_001341729.1:p.Val222=
NM_033507.2:c.669C= NP_277042.1:p.Val223=
NM_033508.2:c.663C= NP_277043.1:p.Val221=
NM_000162.5:c.666C= MANE Select NP_000153.1:p.Val222=
NM_033507.3:c.669C= NP_277042.1:p.Val223=
NM_033508.3:c.663C= NP_277043.1:p.Val221=