Canonical Allele Identifier: CA1703612904
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145599G= , CM000669.2:g.44145599G= GRCh38
NC_000007.13:g.44185198G= , CM000669.1:g.44185198G= GRCh37
NC_000007.12:g.44151723G= NCBI36
NG_008847.1:g.48825C=
NG_008847.2:g.57572C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1149C= ENSP00000379142.4:n.*1149C=
ENST00000616242.5:c.*271C= ENSP00000482149.2:n.*271C=
ENST00000683378.1:n.377C=
ENST00000336642.9:c.185C= ENSP00000338009.5:p.Ala62=
ENST00000345378.7:c.1154C= ENSP00000223366.2:p.Ala385=
ENST00000403799.8:c.1151C= MANE Select ENSP00000384247.3:p.Ala384=
ENST00000671824.1:c.1214C= ENSP00000500264.1:p.Ala405=
ENST00000672743.1:n.163C=
ENST00000673284.1:c.1151C= ENSP00000499852.1:p.Ala384=
ENST00000336642.8:c.203C= ENSP00000338009.4:p.Ala68=
ENST00000345378.6:c.1154C= ENSP00000223366.2:p.Ala385=
ENST00000395796.7:c.1148C= ENSP00000379142.3:p.Ala383=
ENST00000403799.7:c.1151C= ENSP00000384247.3:p.Ala384=
ENST00000437084.1:c.1100C= ENSP00000402840.1:p.Ala367=
ENST00000459642.1:n.531C=
ENST00000616242.4:c.1148C= ENSP00000482149.1:p.Ala383=
NM_000162.3:c.1151C= NP_000153.1:p.Ala384=
NM_033507.1:c.1154C= NP_277042.1:p.Ala385=
NM_033508.1:c.1148C= NP_277043.1:p.Ala383=
NM_000162.4:c.1151C= NP_000153.1:p.Ala384=
NM_001354800.1:c.1151C= NP_001341729.1:p.Ala384=
NM_001354801.1:c.140C= NP_001341730.1:p.Ala47=
NM_001354802.1:c.11C= NP_001341731.1:p.Ala4=
NM_001354803.1:c.185C= NP_001341732.1:p.Ala62=
NM_033507.2:c.1154C= NP_277042.1:p.Ala385=
NM_033508.2:c.1148C= NP_277043.1:p.Ala383=
XM_024446707.1:c.11C= XP_024302475.1:p.Ala4=
NM_000162.5:c.1151C= MANE Select NP_000153.1:p.Ala384=
NM_033507.3:c.1154C= NP_277042.1:p.Ala385=
NM_033508.3:c.1148C= NP_277043.1:p.Ala383=
NM_001354803.2:c.185C= NP_001341732.1:p.Ala62=