Canonical Allele Identifier: CA1846334415

Gene: GNE CLTA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36223424C= , CM000671.2:g.36223424C=	GRCh38
NC_000009.11:g.36223421C= , CM000671.1:g.36223421C=	GRCh37
NC_000009.10:g.36213421C=	NCBI36
NG_008246.1:g.58621G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.1453G= (GNE) MANE Plus Clinical	ENSP00000379839.3:p.Val485=
ENST00000543356.7:c.1183G= (GNE)	ENSP00000437765.3:p.Val395=
ENST00000642385.2:c.1360G= (GNE) MANE Select	ENSP00000494141.2:p.Val454=
ENST00000377902.5:c.1360G= (GNE)	ENSP00000367134.4:p.Val454=
ENST00000396594.7:c.1453G= (GNE)	ENSP00000379839.3:p.Val485=
ENST00000447283.6:c.1360G= (GNE)	ENSP00000414760.2:p.Val454=
ENST00000464497.5:c.485+19245C= (CLTA)	ENSP00000419158.1:n.485+19245C=
ENST00000539208.5:c.1030G= (GNE)	ENSP00000445117.1:p.Val344=
ENST00000539815.5:c.1360G= (GNE)	ENSP00000439155.1:p.Val454=
ENST00000543356.6:c.1345G= (GNE)	ENSP00000437765.2:p.Val449=
NM_001128227.2:c.1453G= (GNE)	NP_001121699.1:p.Val485=
NM_001190383.1:c.1360G= (GNE)	NP_001177312.1:p.Val454=
NM_001190384.1:c.1030G= (GNE)	NP_001177313.1:p.Val344=
NM_001190388.1:c.1345G= (GNE)	NP_001177317.1:p.Val449=
NM_005476.5:c.1360G= (GNE)	NP_005467.1:p.Val454=
XM_005251334.3:c.1300G= (GNE)	XP_005251391.1:p.Val434=
NM_001190383.2:c.1360G= (GNE)	NP_001177312.1:p.Val454=
NM_001190384.2:c.1030G= (GNE)	NP_001177313.1:p.Val344=
NM_005476.6:c.1360G= (GNE)	NP_005467.1:p.Val454=
XM_005251334.4:c.1300G= (GNE)	XP_005251391.1:p.Val434=
XM_017014167.1:c.1360G= (GNE)	XP_016869656.1:p.Val454=
XM_017014168.1:c.1207G= (GNE)	XP_016869657.1:p.Val403=
NM_001128227.3:c.1453G= (GNE) MANE Plus Clinical	NP_001121699.1:p.Val485=
NM_001190383.3:c.1360G= (GNE)	NP_001177312.1:p.Val454=
NM_001190384.3:c.1030G= (GNE)	NP_001177313.1:p.Val344=
NM_001190388.2:c.1183G= (GNE)	NP_001177317.2:p.Val395=
NM_001374797.1:c.1207G= (GNE)	NP_001361726.1:p.Val403=
NM_001374798.1:c.1183G= (GNE)	NP_001361727.1:p.Val395=
NM_005476.7:c.1360G= (GNE) MANE Select	NP_005467.1:p.Val454=