Canonical Allele Identifier: CA1703637521
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153325C= , CM000669.2:g.44153325C= GRCh38
NC_000007.13:g.44192924C= , CM000669.1:g.44192924C= GRCh37
NC_000007.12:g.44159449C= NCBI36
NG_008847.1:g.41099G=
NG_008847.2:g.49846G=

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*182G= ENSP00000379142.4:n.*182G=
ENST00000616242.5:c.184G= ENSP00000482149.2:p.Val62=
ENST00000682635.1:n.670G=
ENST00000345378.7:c.187G= ENSP00000223366.2:p.Val63=
ENST00000403799.8:c.184G= MANE Select ENSP00000384247.3:p.Val62=
ENST00000671824.1:c.184G= ENSP00000500264.1:p.Val62=
ENST00000673284.1:c.184G= ENSP00000499852.1:p.Val62=
ENST00000345378.6:c.187G= ENSP00000223366.2:p.Val63=
ENST00000395796.7:c.181G= ENSP00000379142.3:p.Val61=
ENST00000403799.7:c.184G= ENSP00000384247.3:p.Val62=
ENST00000437084.1:c.184G= ENSP00000402840.1:p.Val62=
ENST00000616242.4:c.181G= ENSP00000482149.1:p.Val61=
NM_000162.3:c.184G= NP_000153.1:p.Val62=
NM_033507.1:c.187G= NP_277042.1:p.Val63=
NM_033508.1:c.181G= NP_277043.1:p.Val61=
NM_000162.4:c.184G= NP_000153.1:p.Val62=
NM_001354800.1:c.184G= NP_001341729.1:p.Val62=
NM_033507.2:c.187G= NP_277042.1:p.Val63=
NM_033508.2:c.181G= NP_277043.1:p.Val61=
NM_000162.5:c.184G= MANE Select NP_000153.1:p.Val62=
NM_033507.3:c.187G= NP_277042.1:p.Val63=
NM_033508.3:c.181G= NP_277043.1:p.Val61=