Canonical Allele Identifier: CA367401890
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44190571T>C (hg19) chr7:g.44150972T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150972T>C , CM000669.2:g.44150972T>C GRCh38
NC_000007.13:g.44190571T>C , CM000669.1:g.44190571T>C GRCh37
NC_000007.12:g.44157096T>C NCBI36
NG_008847.1:g.43452A>G
NG_008847.2:g.52199A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*465A>G ENSP00000379142.4:n.*465A>G
ENST00000616242.5:c.467A>G ENSP00000482149.2:p.His156Arg
ENST00000682635.1:n.953A>G
ENST00000345378.7:c.470A>G ENSP00000223366.2:p.His157Arg
ENST00000403799.8:c.467A>G MANE Select ENSP00000384247.3:p.His156Arg
ENST00000671824.1:c.467A>G ENSP00000500264.1:p.His156Arg
ENST00000673284.1:c.467A>G ENSP00000499852.1:p.His156Arg
ENST00000345378.6:c.470A>G ENSP00000223366.2:p.His157Arg
ENST00000395796.7:c.464A>G ENSP00000379142.3:p.His155Arg
ENST00000403799.7:c.467A>G ENSP00000384247.3:p.His156Arg
ENST00000437084.1:c.416A>G ENSP00000402840.1:p.His139Arg
ENST00000616242.4:c.464A>G ENSP00000482149.1:p.His155Arg
NM_000162.3:c.467A>G NP_000153.1:p.His156Arg
NM_033507.1:c.470A>G NP_277042.1:p.His157Arg
NM_033508.1:c.464A>G NP_277043.1:p.His155Arg
NM_000162.4:c.467A>G NP_000153.1:p.His156Arg
NM_001354800.1:c.467A>G NP_001341729.1:p.His156Arg
NM_033507.2:c.470A>G NP_277042.1:p.His157Arg
NM_033508.2:c.464A>G NP_277043.1:p.His155Arg
NM_000162.5:c.467A>G MANE Select NP_000153.1:p.His156Arg
NM_033507.3:c.470A>G NP_277042.1:p.His157Arg
NM_033508.3:c.464A>G NP_277043.1:p.His155Arg
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