Canonical Allele Identifier: CA1703612464
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44144797G= , CM000669.2:g.44144797G= GRCh38
NC_000007.13:g.44184396G= , CM000669.1:g.44184396G= GRCh37
NC_000007.12:g.44150921G= NCBI36
NG_008847.1:g.49627C=
NG_008847.2:g.58374C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1735C= ENSP00000379142.4:n.*1735C=
ENST00000616242.5:c.*857C= ENSP00000482149.2:n.*857C=
ENST00000683378.1:n.963C=
ENST00000336642.9:c.*339C= ENSP00000338009.5:n.*339C=
ENST00000345378.7:c.*339C= ENSP00000223366.2:n.*339C=
ENST00000403799.8:c.*339C= MANE Select ENSP00000384247.3:n.*339C=
ENST00000671824.1:c.*339C= ENSP00000500264.1:n.*339C=
ENST00000672743.1:n.381+368C=
ENST00000673284.1:c.1369+368C= ENSP00000499852.1:n.1369+368C=
ENST00000336642.8:c.789C= ENSP00000338009.4:n.789C=
ENST00000345378.6:c.*339C= ENSP00000223366.2:n.*339C=
ENST00000395796.7:c.*339C= ENSP00000379142.3:n.*339C=
ENST00000403799.7:c.*339C= ENSP00000384247.3:n.*339C=
ENST00000459642.1:n.1117C=
ENST00000616242.4:c.1734C= ENSP00000482149.1:n.1734C=
NM_000162.3:c.*339C= NP_000153.1:n.*339C=
NM_033507.1:c.*339C= NP_277042.1:n.*339C=
NM_033508.1:c.*339C= NP_277043.1:n.*339C=
NM_000162.4:c.*339C= NP_000153.1:n.*339C=
NM_001354800.1:c.1369+368C= NP_001341729.1:n.1369+368C=
NM_001354801.1:c.*339C= NP_001341730.1:n.*339C=
NM_001354802.1:c.229+368C= NP_001341731.1:n.229+368C=
NM_001354803.1:c.*339C= NP_001341732.1:n.*339C=
NM_033507.2:c.*339C= NP_277042.1:n.*339C=
NM_033508.2:c.*339C= NP_277043.1:n.*339C=
XM_024446707.1:c.*339C= XP_024302475.1:n.*339C=
NM_000162.5:c.*339C= MANE Select NP_000153.1:n.*339C=
NM_033507.3:c.*339C= NP_277042.1:n.*339C=
NM_033508.3:c.*339C= NP_277043.1:n.*339C=
NM_001354803.2:c.*339C= NP_001341732.1:n.*339C=