Canonical Allele Identifier: CA367399409
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145728T>A , CM000669.2:g.44145728T>A GRCh38
NC_000007.13:g.44185327T>A , CM000669.1:g.44185327T>A GRCh37
NC_000007.12:g.44151852T>A NCBI36
NG_008847.1:g.48696A>T
NG_008847.2:g.57443A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1020A>T ENSP00000379142.4:n.*1020A>T
ENST00000616242.5:c.*142A>T ENSP00000482149.2:n.*142A>T
ENST00000683378.1:n.248A>T
ENST00000336642.9:c.56A>T ENSP00000338009.5:p.Asp19Val
ENST00000345378.7:c.1025A>T ENSP00000223366.2:p.Asp342Val
ENST00000403799.8:c.1022A>T MANE Select ENSP00000384247.3:p.Asp341Val
ENST00000671824.1:c.1085A>T ENSP00000500264.1:p.Asp362Val
ENST00000672743.1:n.34A>T
ENST00000673284.1:c.1022A>T ENSP00000499852.1:p.Asp341Val
ENST00000336642.8:c.74A>T ENSP00000338009.4:p.Asp25Val
ENST00000345378.6:c.1025A>T ENSP00000223366.2:p.Asp342Val
ENST00000395796.7:c.1019A>T ENSP00000379142.3:p.Asp340Val
ENST00000403799.7:c.1022A>T ENSP00000384247.3:p.Asp341Val
ENST00000437084.1:c.971A>T ENSP00000402840.1:p.Asp324Val
ENST00000459642.1:n.402A>T
ENST00000473353.1:n.320A>T
ENST00000616242.4:c.1019A>T ENSP00000482149.1:p.Asp340Val
NM_000162.3:c.1022A>T NP_000153.1:p.Asp341Val
NM_033507.1:c.1025A>T NP_277042.1:p.Asp342Val
NM_033508.1:c.1019A>T NP_277043.1:p.Asp340Val
NM_000162.4:c.1022A>T NP_000153.1:p.Asp341Val
NM_001354800.1:c.1022A>T NP_001341729.1:p.Asp341Val
NM_001354801.1:c.11A>T NP_001341730.1:p.Asp4Val
NM_001354802.1:c.-119A>T NP_001341731.1:n.-119A>T
NM_001354803.1:c.56A>T NP_001341732.1:p.Asp19Val
NM_033507.2:c.1025A>T NP_277042.1:p.Asp342Val
NM_033508.2:c.1019A>T NP_277043.1:p.Asp340Val
XM_024446707.1:c.-119A>T XP_024302475.1:n.-119A>T
NM_000162.5:c.1022A>T MANE Select NP_000153.1:p.Asp341Val
NM_033507.3:c.1025A>T NP_277042.1:p.Asp342Val
NM_033508.3:c.1019A>T NP_277043.1:p.Asp340Val
NM_001354803.2:c.56A>T NP_001341732.1:p.Asp19Val