Canonical Allele Identifier: CA2842717516

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146501del , CM000669.2:g.44146501del	GRCh38
NC_000007.13:g.44186100del , CM000669.1:g.44186100del	GRCh37
NC_000007.12:g.44152625del	NCBI36
NG_008847.1:g.47923del
NG_008847.2:g.56670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*979del	ENSP00000379142.4:n.*979del
ENST00000616242.5:c.*101del	ENSP00000482149.2:n.*101del
ENST00000683378.1:n.207del
ENST00000345378.7:c.984del	ENSP00000223366.2:p.Gly329GlufsTer25
ENST00000403799.8:c.981del MANE Select	ENSP00000384247.3:p.Gly328GlufsTer25
ENST00000671824.1:c.1044del	ENSP00000500264.1:p.Gly349GlufsTer25
ENST00000673284.1:c.981del	ENSP00000499852.1:p.Gly328GlufsTer25
ENST00000345378.6:c.984del	ENSP00000223366.2:p.Gly329GlufsTer25
ENST00000395796.7:c.978del	ENSP00000379142.3:p.Gly327GlufsTer25
ENST00000403799.7:c.981del	ENSP00000384247.3:p.Gly328GlufsTer25
ENST00000437084.1:c.930del	ENSP00000402840.1:p.Gly311GlufsTer25
ENST00000473353.1:n.279del
ENST00000616242.4:c.978del	ENSP00000482149.1:p.Gly327GlufsTer25
NM_000162.3:c.981del	NP_000153.1:p.Gly328GlufsTer25
NM_033507.1:c.984del	NP_277042.1:p.Gly329GlufsTer25
NM_033508.1:c.978del	NP_277043.1:p.Gly327GlufsTer25
NM_000162.4:c.981del	NP_000153.1:p.Gly328GlufsTer25
NM_001354800.1:c.981del	NP_001341729.1:p.Gly328GlufsTer25
NM_001354801.1:c.8+118del	NP_001341730.1:n.8+118del
NM_033507.2:c.984del	NP_277042.1:p.Gly329GlufsTer25
NM_033508.2:c.978del	NP_277043.1:p.Gly327GlufsTer25
NM_000162.5:c.981del MANE Select	NP_000153.1:p.Gly328GlufsTer25
NM_033507.3:c.984del	NP_277042.1:p.Gly329GlufsTer25
NM_033508.3:c.978del	NP_277043.1:p.Gly327GlufsTer25