Canonical Allele Identifier: CA2695203102

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147744dup , CM000669.2:g.44147744dup	GRCh38
NC_000007.13:g.44187343dup , CM000669.1:g.44187343dup	GRCh37
NC_000007.12:g.44153868dup	NCBI36
NG_008847.1:g.46680dup
NG_008847.2:g.55427dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*767dup	ENSP00000379142.4:n.*767dup
ENST00000616242.5:c.769dup	ENSP00000482149.2:p.Trp257LeufsTer18
ENST00000345378.7:c.772dup	ENSP00000223366.2:p.Trp258LeufsTer18
ENST00000403799.8:c.769dup MANE Select	ENSP00000384247.3:p.Trp257LeufsTer18
ENST00000671824.1:c.769dup	ENSP00000500264.1:p.Trp257LeufsTer18
ENST00000673284.1:c.769dup	ENSP00000499852.1:p.Trp257LeufsTer18
ENST00000345378.6:c.772dup	ENSP00000223366.2:p.Trp258LeufsTer18
ENST00000395796.7:c.766dup	ENSP00000379142.3:p.Trp256LeufsTer18
ENST00000403799.7:c.769dup	ENSP00000384247.3:p.Trp257LeufsTer18
ENST00000437084.1:c.718dup	ENSP00000402840.1:p.Trp240LeufsTer18
ENST00000616242.4:c.766dup	ENSP00000482149.1:p.Trp256LeufsTer18
NM_000162.3:c.769dup	NP_000153.1:p.Trp257LeufsTer18
NM_033507.1:c.772dup	NP_277042.1:p.Trp258LeufsTer18
NM_033508.1:c.766dup	NP_277043.1:p.Trp256LeufsTer18
XR_927223.1:n.78dup
NM_000162.4:c.769dup	NP_000153.1:p.Trp257LeufsTer18
NM_001354800.1:c.769dup	NP_001341729.1:p.Trp257LeufsTer18
NM_033507.2:c.772dup	NP_277042.1:p.Trp258LeufsTer18
NM_033508.2:c.766dup	NP_277043.1:p.Trp256LeufsTer18
XR_927223.2:n.78dup
NM_000162.5:c.769dup MANE Select	NP_000153.1:p.Trp257LeufsTer18
NM_033507.3:c.772dup	NP_277042.1:p.Trp258LeufsTer18
NM_033508.3:c.766dup	NP_277043.1:p.Trp256LeufsTer18