Canonical Allele Identifier: CA1703634954
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147812T= , CM000669.2:g.44147812T= GRCh38
NC_000007.13:g.44187411T= , CM000669.1:g.44187411T= GRCh37
NC_000007.12:g.44153936T= NCBI36
NG_008847.1:g.46612A=
NG_008847.2:g.55359A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*699A= ENSP00000379142.4:n.*699A=
ENST00000616242.5:c.701A= ENSP00000482149.2:p.Tyr234=
ENST00000345378.7:c.704A= ENSP00000223366.2:p.Tyr235=
ENST00000403799.8:c.701A= MANE Select ENSP00000384247.3:p.Tyr234=
ENST00000671824.1:c.701A= ENSP00000500264.1:p.Tyr234=
ENST00000673284.1:c.701A= ENSP00000499852.1:p.Tyr234=
ENST00000345378.6:c.704A= ENSP00000223366.2:p.Tyr235=
ENST00000395796.7:c.698A= ENSP00000379142.3:p.Tyr233=
ENST00000403799.7:c.701A= ENSP00000384247.3:p.Tyr234=
ENST00000437084.1:c.650A= ENSP00000402840.1:p.Tyr217=
ENST00000616242.4:c.698A= ENSP00000482149.1:p.Tyr233=
NM_000162.3:c.701A= NP_000153.1:p.Tyr234=
NM_033507.1:c.704A= NP_277042.1:p.Tyr235=
NM_033508.1:c.698A= NP_277043.1:p.Tyr233=
XR_927223.1:n.82+64T=
NM_000162.4:c.701A= NP_000153.1:p.Tyr234=
NM_001354800.1:c.701A= NP_001341729.1:p.Tyr234=
NM_033507.2:c.704A= NP_277042.1:p.Tyr235=
NM_033508.2:c.698A= NP_277043.1:p.Tyr233=
XR_927223.2:n.82+64T=
NM_000162.5:c.701A= MANE Select NP_000153.1:p.Tyr234=
NM_033507.3:c.704A= NP_277042.1:p.Tyr235=
NM_033508.3:c.698A= NP_277043.1:p.Tyr233=