Canonical Allele Identifier: CA367402092
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44190632T>G (hg19) chr7:g.44151033T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151033T>G , CM000669.2:g.44151033T>G GRCh38
NC_000007.13:g.44190632T>G , CM000669.1:g.44190632T>G GRCh37
NC_000007.12:g.44157157T>G NCBI36
NG_008847.1:g.43391A>C
NG_008847.2:g.52138A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*404A>C ENSP00000379142.4:n.*404A>C
ENST00000616242.5:c.406A>C ENSP00000482149.2:p.Lys136Gln
ENST00000682635.1:n.892A>C
ENST00000345378.7:c.409A>C ENSP00000223366.2:p.Lys137Gln
ENST00000403799.8:c.406A>C MANE Select ENSP00000384247.3:p.Lys136Gln
ENST00000671824.1:c.406A>C ENSP00000500264.1:p.Lys136Gln
ENST00000673284.1:c.406A>C ENSP00000499852.1:p.Lys136Gln
ENST00000345378.6:c.409A>C ENSP00000223366.2:p.Lys137Gln
ENST00000395796.7:c.403A>C ENSP00000379142.3:p.Lys135Gln
ENST00000403799.7:c.406A>C ENSP00000384247.3:p.Lys136Gln
ENST00000437084.1:c.364-9A>C ENSP00000402840.1:n.364-9A>C
ENST00000616242.4:c.403A>C ENSP00000482149.1:p.Lys135Gln
NM_000162.3:c.406A>C NP_000153.1:p.Lys136Gln
NM_033507.1:c.409A>C NP_277042.1:p.Lys137Gln
NM_033508.1:c.403A>C NP_277043.1:p.Lys135Gln
NM_000162.4:c.406A>C NP_000153.1:p.Lys136Gln
NM_001354800.1:c.406A>C NP_001341729.1:p.Lys136Gln
NM_033507.2:c.409A>C NP_277042.1:p.Lys137Gln
NM_033508.2:c.403A>C NP_277043.1:p.Lys135Gln
NM_000162.5:c.406A>C MANE Select NP_000153.1:p.Lys136Gln
NM_033507.3:c.409A>C NP_277042.1:p.Lys137Gln
NM_033508.3:c.403A>C NP_277043.1:p.Lys135Gln
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