Canonical Allele Identifier: CA1703637056
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44152333C= , CM000669.2:g.44152333C= GRCh38
NC_000007.13:g.44191932C= , CM000669.1:g.44191932C= GRCh37
NC_000007.12:g.44158457C= NCBI36
NG_008847.1:g.42091G=
NG_008847.2:g.50838G=

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*299G= ENSP00000379142.4:n.*299G=
ENST00000616242.5:c.301G= ENSP00000482149.2:p.Val101=
ENST00000682635.1:n.787G=
ENST00000345378.7:c.304G= ENSP00000223366.2:p.Val102=
ENST00000403799.8:c.301G= MANE Select ENSP00000384247.3:p.Val101=
ENST00000671824.1:c.301G= ENSP00000500264.1:p.Val101=
ENST00000673284.1:c.301G= ENSP00000499852.1:p.Val101=
ENST00000345378.6:c.304G= ENSP00000223366.2:p.Val102=
ENST00000395796.7:c.298G= ENSP00000379142.3:p.Val100=
ENST00000403799.7:c.301G= ENSP00000384247.3:p.Val101=
ENST00000437084.1:c.301G= ENSP00000402840.1:p.Val101=
ENST00000616242.4:c.298G= ENSP00000482149.1:p.Val100=
NM_000162.3:c.301G= NP_000153.1:p.Val101=
NM_033507.1:c.304G= NP_277042.1:p.Val102=
NM_033508.1:c.298G= NP_277043.1:p.Val100=
NM_000162.4:c.301G= NP_000153.1:p.Val101=
NM_001354800.1:c.301G= NP_001341729.1:p.Val101=
NM_033507.2:c.304G= NP_277042.1:p.Val102=
NM_033508.2:c.298G= NP_277043.1:p.Val100=
NM_000162.5:c.301G= MANE Select NP_000153.1:p.Val101=
NM_033507.3:c.304G= NP_277042.1:p.Val102=
NM_033508.3:c.298G= NP_277043.1:p.Val100=