Canonical Allele Identifier: CA367399362
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44145719-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145719T>A , CM000669.2:g.44145719T>A GRCh38
NC_000007.13:g.44185318T>A , CM000669.1:g.44185318T>A GRCh37
NC_000007.12:g.44151843T>A NCBI36
NG_008847.1:g.48705A>T
NG_008847.2:g.57452A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1029A>T ENSP00000379142.4:n.*1029A>T
ENST00000616242.5:c.*151A>T ENSP00000482149.2:n.*151A>T
ENST00000683378.1:n.257A>T
ENST00000336642.9:c.65A>T ENSP00000338009.5:p.Asp22Val
ENST00000345378.7:c.1034A>T ENSP00000223366.2:p.Asp345Val
ENST00000403799.8:c.1031A>T MANE Select ENSP00000384247.3:p.Asp344Val
ENST00000671824.1:c.1094A>T ENSP00000500264.1:p.Asp365Val
ENST00000672743.1:n.43A>T
ENST00000673284.1:c.1031A>T ENSP00000499852.1:p.Asp344Val
ENST00000336642.8:c.83A>T ENSP00000338009.4:p.Asp28Val
ENST00000345378.6:c.1034A>T ENSP00000223366.2:p.Asp345Val
ENST00000395796.7:c.1028A>T ENSP00000379142.3:p.Asp343Val
ENST00000403799.7:c.1031A>T ENSP00000384247.3:p.Asp344Val
ENST00000437084.1:c.980A>T ENSP00000402840.1:p.Asp327Val
ENST00000459642.1:n.411A>T
ENST00000473353.1:n.329A>T
ENST00000616242.4:c.1028A>T ENSP00000482149.1:p.Asp343Val
NM_000162.3:c.1031A>T NP_000153.1:p.Asp344Val
NM_033507.1:c.1034A>T NP_277042.1:p.Asp345Val
NM_033508.1:c.1028A>T NP_277043.1:p.Asp343Val
NM_000162.4:c.1031A>T NP_000153.1:p.Asp344Val
NM_001354800.1:c.1031A>T NP_001341729.1:p.Asp344Val
NM_001354801.1:c.20A>T NP_001341730.1:p.Asp7Val
NM_001354802.1:c.-110A>T NP_001341731.1:n.-110A>T
NM_001354803.1:c.65A>T NP_001341732.1:p.Asp22Val
NM_033507.2:c.1034A>T NP_277042.1:p.Asp345Val
NM_033508.2:c.1028A>T NP_277043.1:p.Asp343Val
XM_024446707.1:c.-110A>T XP_024302475.1:n.-110A>T
NM_000162.5:c.1031A>T MANE Select NP_000153.1:p.Asp344Val
NM_033507.3:c.1034A>T NP_277042.1:p.Asp345Val
NM_033508.3:c.1028A>T NP_277043.1:p.Asp343Val
NM_001354803.2:c.65A>T NP_001341732.1:p.Asp22Val