Canonical Allele Identifier: CA1703634854
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147630G= , CM000669.2:g.44147630G= GRCh38
NC_000007.13:g.44187229G= , CM000669.1:g.44187229G= GRCh37
NC_000007.12:g.44153754G= NCBI36
NG_008847.1:g.46794C=
NG_008847.2:g.55541C=

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*861+20C= ENSP00000379142.4:n.*861+20C=
ENST00000616242.5:c.853+30C= ENSP00000482149.2:n.853+30C=
ENST00000345378.7:c.866+20C= ENSP00000223366.2:n.866+20C=
ENST00000403799.8:c.863+20C= MANE Select ENSP00000384247.3:n.863+20C=
ENST00000671824.1:c.853+30C= ENSP00000500264.1:n.853+30C=
ENST00000673284.1:c.863+20C= ENSP00000499852.1:n.863+20C=
ENST00000345378.6:c.866+20C= ENSP00000223366.2:n.866+20C=
ENST00000395796.7:c.860+20C= ENSP00000379142.3:n.860+20C=
ENST00000403799.7:c.863+20C= ENSP00000384247.3:n.863+20C=
ENST00000437084.1:c.812+20C= ENSP00000402840.1:n.812+20C=
ENST00000616242.4:c.860+20C= ENSP00000482149.1:n.860+20C=
NM_000162.3:c.863+20C= NP_000153.1:n.863+20C=
NM_033507.1:c.866+20C= NP_277042.1:n.866+20C=
NM_033508.1:c.860+20C= NP_277043.1:n.860+20C=
NM_000162.4:c.863+20C= NP_000153.1:n.863+20C=
NM_001354800.1:c.863+20C= NP_001341729.1:n.863+20C=
NM_033507.2:c.866+20C= NP_277042.1:n.866+20C=
NM_033508.2:c.860+20C= NP_277043.1:n.860+20C=
NM_000162.5:c.863+20C= MANE Select NP_000153.1:n.863+20C=
NM_033507.3:c.866+20C= NP_277042.1:n.866+20C=
NM_033508.3:c.860+20C= NP_277043.1:n.860+20C=