Canonical Allele Identifier: CA1703612862
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145538G= , CM000669.2:g.44145538G= GRCh38
NC_000007.13:g.44185137G= , CM000669.1:g.44185137G= GRCh37
NC_000007.12:g.44151662G= NCBI36
NG_008847.1:g.48886C=
NG_008847.2:g.57633C=

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*1210C= ENSP00000379142.4:n.*1210C=
ENST00000616242.5:c.*332C= ENSP00000482149.2:n.*332C=
ENST00000683378.1:n.438C=
ENST00000336642.9:c.246C= ENSP00000338009.5:p.Ile82=
ENST00000345378.7:c.1215C= ENSP00000223366.2:p.Ile405=
ENST00000403799.8:c.1212C= MANE Select ENSP00000384247.3:p.Ile404=
ENST00000671824.1:c.1275C= ENSP00000500264.1:p.Ile425=
ENST00000672743.1:n.224C=
ENST00000673284.1:c.1212C= ENSP00000499852.1:p.Ile404=
ENST00000336642.8:c.264C= ENSP00000338009.4:p.Ile88=
ENST00000345378.6:c.1215C= ENSP00000223366.2:p.Ile405=
ENST00000395796.7:c.1209C= ENSP00000379142.3:p.Ile403=
ENST00000403799.7:c.1212C= ENSP00000384247.3:p.Ile404=
ENST00000437084.1:c.1161C= ENSP00000402840.1:p.Ile387=
ENST00000459642.1:n.592C=
ENST00000616242.4:c.1209C= ENSP00000482149.1:p.Ile403=
NM_000162.3:c.1212C= NP_000153.1:p.Ile404=
NM_033507.1:c.1215C= NP_277042.1:p.Ile405=
NM_033508.1:c.1209C= NP_277043.1:p.Ile403=
NM_000162.4:c.1212C= NP_000153.1:p.Ile404=
NM_001354800.1:c.1212C= NP_001341729.1:p.Ile404=
NM_001354801.1:c.201C= NP_001341730.1:p.Ile67=
NM_001354802.1:c.72C= NP_001341731.1:p.Ile24=
NM_001354803.1:c.246C= NP_001341732.1:p.Ile82=
NM_033507.2:c.1215C= NP_277042.1:p.Ile405=
NM_033508.2:c.1209C= NP_277043.1:p.Ile403=
XM_024446707.1:c.72C= XP_024302475.1:p.Ile24=
NM_000162.5:c.1212C= MANE Select NP_000153.1:p.Ile404=
NM_033507.3:c.1215C= NP_277042.1:p.Ile405=
NM_033508.3:c.1209C= NP_277043.1:p.Ile403=
NM_001354803.2:c.246C= NP_001341732.1:p.Ile82=