Canonical Allele Identifier: CA1703612505
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44144898C= , CM000669.2:g.44144898C= GRCh38
NC_000007.13:g.44184497C= , CM000669.1:g.44184497C= GRCh37
NC_000007.12:g.44151022C= NCBI36
NG_008847.1:g.49526G=
NG_008847.2:g.58273G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1634G= ENSP00000379142.4:n.*1634G=
ENST00000616242.5:c.*756G= ENSP00000482149.2:n.*756G=
ENST00000683378.1:n.862G=
ENST00000336642.9:c.*238G= ENSP00000338009.5:n.*238G=
ENST00000345378.7:c.*238G= ENSP00000223366.2:n.*238G=
ENST00000403799.8:c.*238G= MANE Select ENSP00000384247.3:n.*238G=
ENST00000671824.1:c.*238G= ENSP00000500264.1:n.*238G=
ENST00000672743.1:n.381+267G=
ENST00000673284.1:c.1369+267G= ENSP00000499852.1:n.1369+267G=
ENST00000336642.8:c.688G= ENSP00000338009.4:n.688G=
ENST00000345378.6:c.*238G= ENSP00000223366.2:n.*238G=
ENST00000395796.7:c.*238G= ENSP00000379142.3:n.*238G=
ENST00000403799.7:c.*238G= ENSP00000384247.3:n.*238G=
ENST00000459642.1:n.1016G=
ENST00000616242.4:c.1633G= ENSP00000482149.1:n.1633G=
NM_000162.3:c.*238G= NP_000153.1:n.*238G=
NM_033507.1:c.*238G= NP_277042.1:n.*238G=
NM_033508.1:c.*238G= NP_277043.1:n.*238G=
NM_000162.4:c.*238G= NP_000153.1:n.*238G=
NM_001354800.1:c.1369+267G= NP_001341729.1:n.1369+267G=
NM_001354801.1:c.*238G= NP_001341730.1:n.*238G=
NM_001354802.1:c.229+267G= NP_001341731.1:n.229+267G=
NM_001354803.1:c.*238G= NP_001341732.1:n.*238G=
NM_033507.2:c.*238G= NP_277042.1:n.*238G=
NM_033508.2:c.*238G= NP_277043.1:n.*238G=
XM_024446707.1:c.*238G= XP_024302475.1:n.*238G=
NM_000162.5:c.*238G= MANE Select NP_000153.1:n.*238G=
NM_033507.3:c.*238G= NP_277042.1:n.*238G=
NM_033508.3:c.*238G= NP_277043.1:n.*238G=
NM_001354803.2:c.*238G= NP_001341732.1:n.*238G=
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