Canonical Allele Identifier: CA367402107
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44190637A>G (hg19) chr7:g.44151038A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151038A>G , CM000669.2:g.44151038A>G GRCh38
NC_000007.13:g.44190637A>G , CM000669.1:g.44190637A>G GRCh37
NC_000007.12:g.44157162A>G NCBI36
NG_008847.1:g.43386T>C
NG_008847.2:g.52133T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*399T>C ENSP00000379142.4:n.*399T>C
ENST00000616242.5:c.401T>C ENSP00000482149.2:p.Leu134Pro
ENST00000682635.1:n.887T>C
ENST00000345378.7:c.404T>C ENSP00000223366.2:p.Leu135Pro
ENST00000403799.8:c.401T>C MANE Select ENSP00000384247.3:p.Leu134Pro
ENST00000671824.1:c.401T>C ENSP00000500264.1:p.Leu134Pro
ENST00000673284.1:c.401T>C ENSP00000499852.1:p.Leu134Pro
ENST00000345378.6:c.404T>C ENSP00000223366.2:p.Leu135Pro
ENST00000395796.7:c.398T>C ENSP00000379142.3:p.Leu133Pro
ENST00000403799.7:c.401T>C ENSP00000384247.3:p.Leu134Pro
ENST00000437084.1:c.364-14T>C ENSP00000402840.1:n.364-14T>C
ENST00000616242.4:c.398T>C ENSP00000482149.1:p.Leu133Pro
NM_000162.3:c.401T>C NP_000153.1:p.Leu134Pro
NM_033507.1:c.404T>C NP_277042.1:p.Leu135Pro
NM_033508.1:c.398T>C NP_277043.1:p.Leu133Pro
NM_000162.4:c.401T>C NP_000153.1:p.Leu134Pro
NM_001354800.1:c.401T>C NP_001341729.1:p.Leu134Pro
NM_033507.2:c.404T>C NP_277042.1:p.Leu135Pro
NM_033508.2:c.398T>C NP_277043.1:p.Leu133Pro
NM_000162.5:c.401T>C MANE Select NP_000153.1:p.Leu134Pro
NM_033507.3:c.404T>C NP_277042.1:p.Leu135Pro
NM_033508.3:c.398T>C NP_277043.1:p.Leu133Pro
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