Canonical Allele Identifier: CA373426776

Gene: GNE CLTA

Linked Data

• MyVariant Identifiers: chr9:g.36222948G>C (hg19) ; chr9:g.36222951G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36222951G>C , CM000671.2:g.36222951G>C	GRCh38
NC_000009.11:g.36222948G>C , CM000671.1:g.36222948G>C	GRCh37
NC_000009.10:g.36212948G>C	NCBI36
NG_008246.1:g.59094C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.1552C>G (GNE) MANE Plus Clinical	ENSP00000379839.3:p.His518Asp
ENST00000543356.7:c.1282C>G (GNE)	ENSP00000437765.3:p.His428Asp
ENST00000642385.2:c.1459C>G (GNE) MANE Select	ENSP00000494141.2:p.His487Asp
ENST00000377902.5:c.1459C>G (GNE)	ENSP00000367134.4:p.His487Asp
ENST00000396594.7:c.1552C>G (GNE)	ENSP00000379839.3:p.His518Asp
ENST00000447283.6:c.1411+422C>G (GNE)	ENSP00000414760.2:n.1411+422C>G
ENST00000464497.5:c.485+18772G>C (CLTA)	ENSP00000419158.1:n.485+18772G>C
ENST00000539208.5:c.1129C>G (GNE)	ENSP00000445117.1:p.His377Asp
ENST00000539815.5:c.1459C>G (GNE)	ENSP00000439155.1:p.His487Asp
ENST00000543356.6:c.1444C>G (GNE)	ENSP00000437765.2:p.His482Asp
NM_001128227.2:c.1552C>G (GNE)	NP_001121699.1:p.His518Asp
NM_001190383.1:c.1411+422C>G (GNE)	NP_001177312.1:n.1411+422C>G
NM_001190384.1:c.1129C>G (GNE)	NP_001177313.1:p.His377Asp
NM_001190388.1:c.1444C>G (GNE)	NP_001177317.1:p.His482Asp
NM_005476.5:c.1459C>G (GNE)	NP_005467.1:p.His487Asp
XM_005251334.3:c.1399C>G (GNE)	XP_005251391.1:p.His467Asp
NM_001190383.2:c.1411+422C>G (GNE)	NP_001177312.1:n.1411+422C>G
NM_001190384.2:c.1129C>G (GNE)	NP_001177313.1:p.His377Asp
NM_005476.6:c.1459C>G (GNE)	NP_005467.1:p.His487Asp
XM_005251334.4:c.1399C>G (GNE)	XP_005251391.1:p.His467Asp
XM_017014167.1:c.1459C>G (GNE)	XP_016869656.1:p.His487Asp
XM_017014168.1:c.1306C>G (GNE)	XP_016869657.1:p.His436Asp
NM_001128227.3:c.1552C>G (GNE) MANE Plus Clinical	NP_001121699.1:p.His518Asp
NM_001190383.3:c.1411+422C>G (GNE)	NP_001177312.1:n.1411+422C>G
NM_001190384.3:c.1129C>G (GNE)	NP_001177313.1:p.His377Asp
NM_001190388.2:c.1282C>G (GNE)	NP_001177317.2:p.His428Asp
NM_001374797.1:c.1306C>G (GNE)	NP_001361726.1:p.His436Asp
NM_001374798.1:c.1282C>G (GNE)	NP_001361727.1:p.His428Asp
NM_005476.7:c.1459C>G (GNE) MANE Select	NP_005467.1:p.His487Asp