Canonical Allele Identifier: CA367397245
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1709730

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145264G>A , CM000669.2:g.44145264G>A GRCh38
NC_000007.13:g.44184863G>A , CM000669.1:g.44184863G>A GRCh37
NC_000007.12:g.44151388G>A NCBI36
NG_008847.1:g.49160C>T
NG_008847.2:g.57907C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1268C>T ENSP00000379142.4:n.*1268C>T
ENST00000616242.5:c.*390C>T ENSP00000482149.2:n.*390C>T
ENST00000683378.1:n.496C>T
ENST00000336642.9:c.304C>T ENSP00000338009.5:p.His102Tyr
ENST00000345378.7:c.1273C>T ENSP00000223366.2:p.His425Tyr
ENST00000403799.8:c.1270C>T MANE Select ENSP00000384247.3:p.His424Tyr
ENST00000671824.1:c.1333C>T ENSP00000500264.1:p.His445Tyr
ENST00000672743.1:n.282C>T
ENST00000673284.1:c.1270C>T ENSP00000499852.1:p.His424Tyr
ENST00000336642.8:c.322C>T ENSP00000338009.4:p.His108Tyr
ENST00000345378.6:c.1273C>T ENSP00000223366.2:p.His425Tyr
ENST00000395796.7:c.1267C>T ENSP00000379142.3:p.His423Tyr
ENST00000403799.7:c.1270C>T ENSP00000384247.3:p.His424Tyr
ENST00000437084.1:c.1219C>T ENSP00000402840.1:p.His407Tyr
ENST00000459642.1:n.650C>T
ENST00000616242.4:c.1267C>T ENSP00000482149.1:p.His423Tyr
NM_000162.3:c.1270C>T NP_000153.1:p.His424Tyr
NM_033507.1:c.1273C>T NP_277042.1:p.His425Tyr
NM_033508.1:c.1267C>T NP_277043.1:p.His423Tyr
NM_000162.4:c.1270C>T NP_000153.1:p.His424Tyr
NM_001354800.1:c.1270C>T NP_001341729.1:p.His424Tyr
NM_001354801.1:c.259C>T NP_001341730.1:p.His87Tyr
NM_001354802.1:c.130C>T NP_001341731.1:p.His44Tyr
NM_001354803.1:c.304C>T NP_001341732.1:p.His102Tyr
NM_033507.2:c.1273C>T NP_277042.1:p.His425Tyr
NM_033508.2:c.1267C>T NP_277043.1:p.His423Tyr
XM_024446707.1:c.130C>T XP_024302475.1:p.His44Tyr
NM_000162.5:c.1270C>T MANE Select NP_000153.1:p.His424Tyr
NM_033507.3:c.1273C>T NP_277042.1:p.His425Tyr
NM_033508.3:c.1267C>T NP_277043.1:p.His423Tyr
NM_001354803.2:c.304C>T NP_001341732.1:p.His102Tyr