Canonical Allele Identifier: CA2695203126
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149762delinsTT , CM000669.2:g.44149762delinsTT GRCh38
NC_000007.13:g.44189361delinsTT , CM000669.1:g.44189361delinsTT GRCh37
NC_000007.12:g.44155886delinsTT NCBI36
NG_008847.1:g.44662delinsAA
NG_008847.2:g.53409delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*675delinsAA ENSP00000379142.4:n.*675delinsAA
ENST00000616242.5:c.677delinsAA ENSP00000482149.2:p.Val226GlufsTer?
ENST00000682635.1:n.1163delinsAA
ENST00000345378.7:c.680delinsAA ENSP00000223366.2:p.Val227GlufsTer?
ENST00000403799.8:c.677delinsAA MANE Select ENSP00000384247.3:p.Val226GlufsTer?
ENST00000671824.1:c.677delinsAA ENSP00000500264.1:p.Val226GlufsTer?
ENST00000673284.1:c.677delinsAA ENSP00000499852.1:p.Val226GlufsTer?
ENST00000345378.6:c.680delinsAA ENSP00000223366.2:p.Val227GlufsTer?
ENST00000395796.7:c.674delinsAA ENSP00000379142.3:p.Val225GlufsTer?
ENST00000403799.7:c.677delinsAA ENSP00000384247.3:p.Val226GlufsTer?
ENST00000437084.1:c.626delinsAA ENSP00000402840.1:p.Val209GlufsTer?
ENST00000616242.4:c.674delinsAA ENSP00000482149.1:p.Val225GlufsTer?
NM_000162.3:c.677delinsAA NP_000153.1:p.Val226GlufsTer?
NM_033507.1:c.680delinsAA NP_277042.1:p.Val227GlufsTer?
NM_033508.1:c.674delinsAA NP_277043.1:p.Val225GlufsTer?
XR_927223.1:n.277delinsTT
NM_000162.4:c.677delinsAA NP_000153.1:p.Val226GlufsTer?
NM_001354800.1:c.677delinsAA NP_001341729.1:p.Val226GlufsTer?
NM_033507.2:c.680delinsAA NP_277042.1:p.Val227GlufsTer?
NM_033508.2:c.674delinsAA NP_277043.1:p.Val225GlufsTer?
XR_927223.2:n.277delinsTT
NM_000162.5:c.677delinsAA MANE Select NP_000153.1:p.Val226GlufsTer?
NM_033507.3:c.680delinsAA NP_277042.1:p.Val227GlufsTer?
NM_033508.3:c.674delinsAA NP_277043.1:p.Val225GlufsTer?