Canonical Allele Identifier: CA367403241
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44192911G>C (hg19) chr7:g.44153312G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153312G>C , CM000669.2:g.44153312G>C GRCh38
NC_000007.13:g.44192911G>C , CM000669.1:g.44192911G>C GRCh37
NC_000007.12:g.44159436G>C NCBI36
NG_008847.1:g.41112C>G
NG_008847.2:g.49859C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*195C>G ENSP00000379142.4:n.*195C>G
ENST00000616242.5:c.197C>G ENSP00000482149.2:p.Pro66Arg
ENST00000682635.1:n.683C>G
ENST00000345378.7:c.200C>G ENSP00000223366.2:p.Pro67Arg
ENST00000403799.8:c.197C>G MANE Select ENSP00000384247.3:p.Pro66Arg
ENST00000671824.1:c.197C>G ENSP00000500264.1:p.Pro66Arg
ENST00000673284.1:c.197C>G ENSP00000499852.1:p.Pro66Arg
ENST00000345378.6:c.200C>G ENSP00000223366.2:p.Pro67Arg
ENST00000395796.7:c.194C>G ENSP00000379142.3:p.Pro65Arg
ENST00000403799.7:c.197C>G ENSP00000384247.3:p.Pro66Arg
ENST00000437084.1:c.197C>G ENSP00000402840.1:p.Pro66Arg
ENST00000616242.4:c.194C>G ENSP00000482149.1:p.Pro65Arg
NM_000162.3:c.197C>G NP_000153.1:p.Pro66Arg
NM_033507.1:c.200C>G NP_277042.1:p.Pro67Arg
NM_033508.1:c.194C>G NP_277043.1:p.Pro65Arg
NM_000162.4:c.197C>G NP_000153.1:p.Pro66Arg
NM_001354800.1:c.197C>G NP_001341729.1:p.Pro66Arg
NM_033507.2:c.200C>G NP_277042.1:p.Pro67Arg
NM_033508.2:c.194C>G NP_277043.1:p.Pro65Arg
NM_000162.5:c.197C>G MANE Select NP_000153.1:p.Pro66Arg
NM_033507.3:c.200C>G NP_277042.1:p.Pro67Arg
NM_033508.3:c.194C>G NP_277043.1:p.Pro65Arg
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