Canonical Allele Identifier: CA1703612637
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145133C= , CM000669.2:g.44145133C= GRCh38
NC_000007.13:g.44184732C= , CM000669.1:g.44184732C= GRCh37
NC_000007.12:g.44151257C= NCBI36
NG_008847.1:g.49291G=
NG_008847.2:g.58038G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1399G= ENSP00000379142.4:n.*1399G=
ENST00000616242.5:c.*521G= ENSP00000482149.2:n.*521G=
ENST00000683378.1:n.627G=
ENST00000336642.9:c.*3G= ENSP00000338009.5:n.*3G=
ENST00000345378.7:c.*3G= ENSP00000223366.2:n.*3G=
ENST00000403799.8:c.*3G= MANE Select ENSP00000384247.3:n.*3G=
ENST00000671824.1:c.*3G= ENSP00000500264.1:n.*3G=
ENST00000672743.1:n.381+32G=
ENST00000673284.1:c.1369+32G= ENSP00000499852.1:n.1369+32G=
ENST00000336642.8:c.453G= ENSP00000338009.4:n.453G=
ENST00000345378.6:c.*3G= ENSP00000223366.2:n.*3G=
ENST00000395796.7:c.*3G= ENSP00000379142.3:n.*3G=
ENST00000403799.7:c.*3G= ENSP00000384247.3:n.*3G=
ENST00000437084.1:c.*3G= ENSP00000402840.1:n.*3G=
ENST00000459642.1:n.781G=
ENST00000616242.4:c.1398G= ENSP00000482149.1:n.1398G=
NM_000162.3:c.*3G= NP_000153.1:n.*3G=
NM_033507.1:c.*3G= NP_277042.1:n.*3G=
NM_033508.1:c.*3G= NP_277043.1:n.*3G=
NM_000162.4:c.*3G= NP_000153.1:n.*3G=
NM_001354800.1:c.1369+32G= NP_001341729.1:n.1369+32G=
NM_001354801.1:c.*3G= NP_001341730.1:n.*3G=
NM_001354802.1:c.229+32G= NP_001341731.1:n.229+32G=
NM_001354803.1:c.*3G= NP_001341732.1:n.*3G=
NM_033507.2:c.*3G= NP_277042.1:n.*3G=
NM_033508.2:c.*3G= NP_277043.1:n.*3G=
XM_024446707.1:c.*3G= XP_024302475.1:n.*3G=
NM_000162.5:c.*3G= MANE Select NP_000153.1:n.*3G=
NM_033507.3:c.*3G= NP_277042.1:n.*3G=
NM_033508.3:c.*3G= NP_277043.1:n.*3G=
NM_001354803.2:c.*3G= NP_001341732.1:n.*3G=
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