Canonical Allele Identifier: CA1703635894
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149858T= , CM000669.2:g.44149858T= GRCh38
NC_000007.13:g.44189457T= , CM000669.1:g.44189457T= GRCh37
NC_000007.12:g.44155982T= NCBI36
NG_008847.1:g.44566A=
NG_008847.2:g.53313A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*579A= ENSP00000379142.4:n.*579A=
ENST00000616242.5:c.581A= ENSP00000482149.2:p.Asp194=
ENST00000682635.1:n.1067A=
ENST00000345378.7:c.584A= ENSP00000223366.2:p.Asp195=
ENST00000403799.8:c.581A= MANE Select ENSP00000384247.3:p.Asp194=
ENST00000671824.1:c.581A= ENSP00000500264.1:p.Asp194=
ENST00000673284.1:c.581A= ENSP00000499852.1:p.Asp194=
ENST00000345378.6:c.584A= ENSP00000223366.2:p.Asp195=
ENST00000395796.7:c.578A= ENSP00000379142.3:p.Asp193=
ENST00000403799.7:c.581A= ENSP00000384247.3:p.Asp194=
ENST00000437084.1:c.530A= ENSP00000402840.1:p.Asp177=
ENST00000616242.4:c.578A= ENSP00000482149.1:p.Asp193=
NM_000162.3:c.581A= NP_000153.1:p.Asp194=
NM_033507.1:c.584A= NP_277042.1:p.Asp195=
NM_033508.1:c.578A= NP_277043.1:p.Asp193=
NM_000162.4:c.581A= NP_000153.1:p.Asp194=
NM_001354800.1:c.581A= NP_001341729.1:p.Asp194=
NM_033507.2:c.584A= NP_277042.1:p.Asp195=
NM_033508.2:c.578A= NP_277043.1:p.Asp193=
NM_000162.5:c.581A= MANE Select NP_000153.1:p.Asp194=
NM_033507.3:c.584A= NP_277042.1:p.Asp195=
NM_033508.3:c.578A= NP_277043.1:p.Asp193=
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