Canonical Allele Identifier: CA2695203127

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149768_44149778dup , CM000669.2:g.44149768_44149778dup	GRCh38
NC_000007.13:g.44189367_44189377dup , CM000669.1:g.44189367_44189377dup	GRCh37
NC_000007.12:g.44155892_44155902dup	NCBI36
NG_008847.1:g.44648_44658dup
NG_008847.2:g.53395_53405dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*661_*671dup	ENSP00000379142.4:n.*661_*671dup
ENST00000616242.5:c.663_673dup	ENSP00000482149.2:p.Ile225ArgfsTer4
ENST00000682635.1:n.1149_1159dup
ENST00000345378.7:c.666_676dup	ENSP00000223366.2:p.Ile226ArgfsTer4
ENST00000403799.8:c.663_673dup MANE Select	ENSP00000384247.3:p.Ile225ArgfsTer4
ENST00000671824.1:c.663_673dup	ENSP00000500264.1:p.Ile225ArgfsTer4
ENST00000673284.1:c.663_673dup	ENSP00000499852.1:p.Ile225ArgfsTer4
ENST00000345378.6:c.666_676dup	ENSP00000223366.2:p.Ile226ArgfsTer4
ENST00000395796.7:c.660_670dup	ENSP00000379142.3:p.Ile224ArgfsTer4
ENST00000403799.7:c.663_673dup	ENSP00000384247.3:p.Ile225ArgfsTer4
ENST00000437084.1:c.612_622dup	ENSP00000402840.1:p.Ile208ArgfsTer4
ENST00000616242.4:c.660_670dup	ENSP00000482149.1:p.Ile224ArgfsTer4
NM_000162.3:c.663_673dup	NP_000153.1:p.Ile225ArgfsTer4
NM_033507.1:c.666_676dup	NP_277042.1:p.Ile226ArgfsTer4
NM_033508.1:c.660_670dup	NP_277043.1:p.Ile224ArgfsTer4
NM_000162.4:c.663_673dup	NP_000153.1:p.Ile225ArgfsTer4
NM_001354800.1:c.663_673dup	NP_001341729.1:p.Ile225ArgfsTer4
NM_033507.2:c.666_676dup	NP_277042.1:p.Ile226ArgfsTer4
NM_033508.2:c.660_670dup	NP_277043.1:p.Ile224ArgfsTer4
NM_000162.5:c.663_673dup MANE Select	NP_000153.1:p.Ile225ArgfsTer4
NM_033507.3:c.666_676dup	NP_277042.1:p.Ile226ArgfsTer4
NM_033508.3:c.660_670dup	NP_277043.1:p.Ile224ArgfsTer4