Canonical Allele Identifier: CA1846326086

Gene: GNE CLTA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36249344_36249347delinsATTC , CM000671.2:g.36249344_36249347delinsATTC	GRCh38
NC_000009.11:g.36249341_36249344delinsATTC , CM000671.1:g.36249341_36249344delinsATTC	GRCh37
NC_000009.10:g.36239341_36239344delinsATTC	NCBI36
NG_008246.1:g.32698_32701delinsGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.102_105delinsGAAT (GNE) MANE Plus Clinical	ENSP00000379839.3:p.Lys34=
ENST00000543356.7:c.-13-2865_-13-2862delinsGAAT (GNE)	ENSP00000437765.3:n.-13-2865_-13-2862delinsGAAT
ENST00000642385.2:c.9_12delinsGAAT (GNE) MANE Select	ENSP00000494141.2:p.Lys3=
ENST00000377902.5:c.9_12delinsGAAT (GNE)	ENSP00000367134.4:p.Lys3=
ENST00000396594.7:c.102_105delinsGAAT (GNE)	ENSP00000379839.3:p.Lys34=
ENST00000447283.6:c.9_12delinsGAAT (GNE)	ENSP00000414760.2:p.Lys3=
ENST00000464497.5:c.486-13854_486-13851delinsATTC (CLTA)	ENSP00000419158.1:n.486-13854_486-13851delinsATTC
ENST00000539208.5:c.-13-2865_-13-2862delinsGAAT (GNE)	ENSP00000445117.1:n.-13-2865_-13-2862delinsGAAT
ENST00000539815.5:c.9_12delinsGAAT (GNE)	ENSP00000439155.1:p.Lys3=
ENST00000543356.6:c.150-2865_150-2862delinsGAAT (GNE)	ENSP00000437765.2:n.150-2865_150-2862delinsGAAT
NM_001128227.2:c.102_105delinsGAAT (GNE)	NP_001121699.1:p.Lys34=
NM_001190383.1:c.9_12delinsGAAT (GNE)	NP_001177312.1:p.Lys3=
NM_001190384.1:c.-13-2865_-13-2862delinsGAAT (GNE)	NP_001177313.1:n.-13-2865_-13-2862delinsGAAT
NM_001190388.1:c.150-2865_150-2862delinsGAAT (GNE)	NP_001177317.1:n.150-2865_150-2862delinsGAAT
NM_005476.5:c.9_12delinsGAAT (GNE)	NP_005467.1:p.Lys3=
XM_005251334.3:c.102_105delinsGAAT (GNE)	XP_005251391.1:p.Lys34=
NM_001190383.2:c.9_12delinsGAAT (GNE)	NP_001177312.1:p.Lys3=
NM_001190384.2:c.-13-2865_-13-2862delinsGAAT (GNE)	NP_001177313.1:n.-13-2865_-13-2862delinsGAAT
NM_005476.6:c.9_12delinsGAAT (GNE)	NP_005467.1:p.Lys3=
XM_005251334.4:c.102_105delinsGAAT (GNE)	XP_005251391.1:p.Lys34=
XM_017014167.1:c.9_12delinsGAAT (GNE)	XP_016869656.1:p.Lys3=
XM_017014168.1:c.9_12delinsGAAT (GNE)	XP_016869657.1:p.Lys3=
NM_001128227.3:c.102_105delinsGAAT (GNE) MANE Plus Clinical	NP_001121699.1:p.Lys34=
NM_001190383.3:c.9_12delinsGAAT (GNE)	NP_001177312.1:p.Lys3=
NM_001190384.3:c.-13-2865_-13-2862delinsGAAT (GNE)	NP_001177313.1:n.-13-2865_-13-2862delinsGAAT
NM_001190388.2:c.-13-2865_-13-2862delinsGAAT (GNE)	NP_001177317.2:n.-13-2865_-13-2862delinsGAAT
NM_001374797.1:c.9_12delinsGAAT (GNE)	NP_001361726.1:p.Lys3=
NM_001374798.1:c.-13-2865_-13-2862delinsGAAT (GNE)	NP_001361727.1:n.-13-2865_-13-2862delinsGAAT
NM_005476.7:c.9_12delinsGAAT (GNE) MANE Select	NP_005467.1:p.Lys3=