Canonical Allele Identifier: CA367399024
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145656T>A , CM000669.2:g.44145656T>A GRCh38
NC_000007.13:g.44185255T>A , CM000669.1:g.44185255T>A GRCh37
NC_000007.12:g.44151780T>A NCBI36
NG_008847.1:g.48768A>T
NG_008847.2:g.57515A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1092A>T ENSP00000379142.4:n.*1092A>T
ENST00000616242.5:c.*214A>T ENSP00000482149.2:n.*214A>T
ENST00000683378.1:n.320A>T
ENST00000336642.9:c.128A>T ENSP00000338009.5:p.Asp43Val
ENST00000345378.7:c.1097A>T ENSP00000223366.2:p.Asp366Val
ENST00000403799.8:c.1094A>T MANE Select ENSP00000384247.3:p.Asp365Val
ENST00000671824.1:c.1157A>T ENSP00000500264.1:p.Asp386Val
ENST00000672743.1:n.106A>T
ENST00000673284.1:c.1094A>T ENSP00000499852.1:p.Asp365Val
ENST00000336642.8:c.146A>T ENSP00000338009.4:p.Asp49Val
ENST00000345378.6:c.1097A>T ENSP00000223366.2:p.Asp366Val
ENST00000395796.7:c.1091A>T ENSP00000379142.3:p.Asp364Val
ENST00000403799.7:c.1094A>T ENSP00000384247.3:p.Asp365Val
ENST00000437084.1:c.1043A>T ENSP00000402840.1:p.Asp348Val
ENST00000459642.1:n.474A>T
ENST00000473353.1:n.392A>T
ENST00000616242.4:c.1091A>T ENSP00000482149.1:p.Asp364Val
NM_000162.3:c.1094A>T NP_000153.1:p.Asp365Val
NM_033507.1:c.1097A>T NP_277042.1:p.Asp366Val
NM_033508.1:c.1091A>T NP_277043.1:p.Asp364Val
NM_000162.4:c.1094A>T NP_000153.1:p.Asp365Val
NM_001354800.1:c.1094A>T NP_001341729.1:p.Asp365Val
NM_001354801.1:c.83A>T NP_001341730.1:p.Asp28Val
NM_001354802.1:c.-47A>T NP_001341731.1:n.-47A>T
NM_001354803.1:c.128A>T NP_001341732.1:p.Asp43Val
NM_033507.2:c.1097A>T NP_277042.1:p.Asp366Val
NM_033508.2:c.1091A>T NP_277043.1:p.Asp364Val
XM_024446707.1:c.-47A>T XP_024302475.1:n.-47A>T
NM_000162.5:c.1094A>T MANE Select NP_000153.1:p.Asp365Val
NM_033507.3:c.1097A>T NP_277042.1:p.Asp366Val
NM_033508.3:c.1091A>T NP_277043.1:p.Asp364Val
NM_001354803.2:c.128A>T NP_001341732.1:p.Asp43Val