Canonical Allele Identifier: CA367402129
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44190643T>A (hg19) chr7:g.44151044T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151044T>A , CM000669.2:g.44151044T>A GRCh38
NC_000007.13:g.44190643T>A , CM000669.1:g.44190643T>A GRCh37
NC_000007.12:g.44157168T>A NCBI36
NG_008847.1:g.43380A>T
NG_008847.2:g.52127A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*393A>T ENSP00000379142.4:n.*393A>T
ENST00000616242.5:c.395A>T ENSP00000482149.2:p.Asp132Val
ENST00000682635.1:n.881A>T
ENST00000345378.7:c.398A>T ENSP00000223366.2:p.Asp133Val
ENST00000403799.8:c.395A>T MANE Select ENSP00000384247.3:p.Asp132Val
ENST00000671824.1:c.395A>T ENSP00000500264.1:p.Asp132Val
ENST00000673284.1:c.395A>T ENSP00000499852.1:p.Asp132Val
ENST00000345378.6:c.398A>T ENSP00000223366.2:p.Asp133Val
ENST00000395796.7:c.392A>T ENSP00000379142.3:p.Asp131Val
ENST00000403799.7:c.395A>T ENSP00000384247.3:p.Asp132Val
ENST00000437084.1:c.364-20A>T ENSP00000402840.1:n.364-20A>T
ENST00000616242.4:c.392A>T ENSP00000482149.1:p.Asp131Val
NM_000162.3:c.395A>T NP_000153.1:p.Asp132Val
NM_033507.1:c.398A>T NP_277042.1:p.Asp133Val
NM_033508.1:c.392A>T NP_277043.1:p.Asp131Val
NM_000162.4:c.395A>T NP_000153.1:p.Asp132Val
NM_001354800.1:c.395A>T NP_001341729.1:p.Asp132Val
NM_033507.2:c.398A>T NP_277042.1:p.Asp133Val
NM_033508.2:c.392A>T NP_277043.1:p.Asp131Val
NM_000162.5:c.395A>T MANE Select NP_000153.1:p.Asp132Val
NM_033507.3:c.398A>T NP_277042.1:p.Asp133Val
NM_033508.3:c.392A>T NP_277043.1:p.Asp131Val
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