Canonical Allele Identifier: CA367401232
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44189390T>G (hg19) chr7:g.44149791T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149791T>G , CM000669.2:g.44149791T>G GRCh38
NC_000007.13:g.44189390T>G , CM000669.1:g.44189390T>G GRCh37
NC_000007.12:g.44155915T>G NCBI36
NG_008847.1:g.44633A>C
NG_008847.2:g.53380A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*646A>C ENSP00000379142.4:n.*646A>C
ENST00000616242.5:c.648A>C ENSP00000482149.2:p.Glu216Asp
ENST00000682635.1:n.1134A>C
ENST00000345378.7:c.651A>C ENSP00000223366.2:p.Glu217Asp
ENST00000403799.8:c.648A>C MANE Select ENSP00000384247.3:p.Glu216Asp
ENST00000671824.1:c.648A>C ENSP00000500264.1:p.Glu216Asp
ENST00000673284.1:c.648A>C ENSP00000499852.1:p.Glu216Asp
ENST00000345378.6:c.651A>C ENSP00000223366.2:p.Glu217Asp
ENST00000395796.7:c.645A>C ENSP00000379142.3:p.Glu215Asp
ENST00000403799.7:c.648A>C ENSP00000384247.3:p.Glu216Asp
ENST00000437084.1:c.597A>C ENSP00000402840.1:p.Glu199Asp
ENST00000616242.4:c.645A>C ENSP00000482149.1:p.Glu215Asp
NM_000162.3:c.648A>C NP_000153.1:p.Glu216Asp
NM_033507.1:c.651A>C NP_277042.1:p.Glu217Asp
NM_033508.1:c.645A>C NP_277043.1:p.Glu215Asp
NM_000162.4:c.648A>C NP_000153.1:p.Glu216Asp
NM_001354800.1:c.648A>C NP_001341729.1:p.Glu216Asp
NM_033507.2:c.651A>C NP_277042.1:p.Glu217Asp
NM_033508.2:c.645A>C NP_277043.1:p.Glu215Asp
NM_000162.5:c.648A>C MANE Select NP_000153.1:p.Glu216Asp
NM_033507.3:c.651A>C NP_277042.1:p.Glu217Asp
NM_033508.3:c.645A>C NP_277043.1:p.Glu215Asp
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