Canonical Allele Identifier: CA1703635887
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149839C= , CM000669.2:g.44149839C= GRCh38
NC_000007.13:g.44189438C= , CM000669.1:g.44189438C= GRCh37
NC_000007.12:g.44155963C= NCBI36
NG_008847.1:g.44585G=
NG_008847.2:g.53332G=

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*598G= ENSP00000379142.4:n.*598G=
ENST00000616242.5:c.600G= ENSP00000482149.2:p.Val200=
ENST00000682635.1:n.1086G=
ENST00000345378.7:c.603G= ENSP00000223366.2:p.Val201=
ENST00000403799.8:c.600G= MANE Select ENSP00000384247.3:p.Val200=
ENST00000671824.1:c.600G= ENSP00000500264.1:p.Val200=
ENST00000673284.1:c.600G= ENSP00000499852.1:p.Val200=
ENST00000345378.6:c.603G= ENSP00000223366.2:p.Val201=
ENST00000395796.7:c.597G= ENSP00000379142.3:p.Val199=
ENST00000403799.7:c.600G= ENSP00000384247.3:p.Val200=
ENST00000437084.1:c.549G= ENSP00000402840.1:p.Val183=
ENST00000616242.4:c.597G= ENSP00000482149.1:p.Val199=
NM_000162.3:c.600G= NP_000153.1:p.Val200=
NM_033507.1:c.603G= NP_277042.1:p.Val201=
NM_033508.1:c.597G= NP_277043.1:p.Val199=
NM_000162.4:c.600G= NP_000153.1:p.Val200=
NM_001354800.1:c.600G= NP_001341729.1:p.Val200=
NM_033507.2:c.603G= NP_277042.1:p.Val201=
NM_033508.2:c.597G= NP_277043.1:p.Val199=
NM_000162.5:c.600G= MANE Select NP_000153.1:p.Val200=
NM_033507.3:c.603G= NP_277042.1:p.Val201=
NM_033508.3:c.597G= NP_277043.1:p.Val199=