Canonical Allele Identifier: CA1703636457
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151002A= , CM000669.2:g.44151002A= GRCh38
NC_000007.13:g.44190601A= , CM000669.1:g.44190601A= GRCh37
NC_000007.12:g.44157126A= NCBI36
NG_008847.1:g.43422T=
NG_008847.2:g.52169T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*435T= ENSP00000379142.4:n.*435T=
ENST00000616242.5:c.437T= ENSP00000482149.2:p.Leu146=
ENST00000682635.1:n.923T=
ENST00000345378.7:c.440T= ENSP00000223366.2:p.Leu147=
ENST00000403799.8:c.437T= MANE Select ENSP00000384247.3:p.Leu146=
ENST00000671824.1:c.437T= ENSP00000500264.1:p.Leu146=
ENST00000673284.1:c.437T= ENSP00000499852.1:p.Leu146=
ENST00000345378.6:c.440T= ENSP00000223366.2:p.Leu147=
ENST00000395796.7:c.434T= ENSP00000379142.3:p.Leu145=
ENST00000403799.7:c.437T= ENSP00000384247.3:p.Leu146=
ENST00000437084.1:c.386T= ENSP00000402840.1:p.Leu129=
ENST00000616242.4:c.434T= ENSP00000482149.1:p.Leu145=
NM_000162.3:c.437T= NP_000153.1:p.Leu146=
NM_033507.1:c.440T= NP_277042.1:p.Leu147=
NM_033508.1:c.434T= NP_277043.1:p.Leu145=
NM_000162.4:c.437T= NP_000153.1:p.Leu146=
NM_001354800.1:c.437T= NP_001341729.1:p.Leu146=
NM_033507.2:c.440T= NP_277042.1:p.Leu147=
NM_033508.2:c.434T= NP_277043.1:p.Leu145=
NM_000162.5:c.437T= MANE Select NP_000153.1:p.Leu146=
NM_033507.3:c.440T= NP_277042.1:p.Leu147=
NM_033508.3:c.434T= NP_277043.1:p.Leu145=
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