Canonical Allele Identifier: CA373417987

Gene: GNE CLTA

Linked Data

• ClinVar Variation Id: 963089
• ClinVar RCV Id: RCV001237063
• dbSNP Id: rs1829857314
• gnomAD v4: 9-36246045-A-T
• MyVariant Identifiers: chr9:g.36246042A>T (hg19) ; chr9:g.36246045A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36246045A>T , CM000671.2:g.36246045A>T	GRCh38
NC_000009.11:g.36246042A>T , CM000671.1:g.36246042A>T	GRCh37
NC_000009.10:g.36236042A>T	NCBI36
NG_008246.1:g.36000T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.695T>A (GNE) MANE Plus Clinical	ENSP00000379839.3:p.Ile232Asn
ENST00000543356.7:c.425T>A (GNE)	ENSP00000437765.3:p.Ile142Asn
ENST00000642385.2:c.602T>A (GNE) MANE Select	ENSP00000494141.2:p.Ile201Asn
ENST00000377902.5:c.602T>A (GNE)	ENSP00000367134.4:p.Ile201Asn
ENST00000396594.7:c.695T>A (GNE)	ENSP00000379839.3:p.Ile232Asn
ENST00000447283.6:c.602T>A (GNE)	ENSP00000414760.2:p.Ile201Asn
ENST00000464497.5:c.486-17153A>T (CLTA)	ENSP00000419158.1:n.486-17153A>T
ENST00000539208.5:c.425T>A (GNE)	ENSP00000445117.1:p.Ile142Asn
ENST00000539815.5:c.602T>A (GNE)	ENSP00000439155.1:p.Ile201Asn
ENST00000543356.6:c.587T>A (GNE)	ENSP00000437765.2:p.Ile196Asn
NM_001128227.2:c.695T>A (GNE)	NP_001121699.1:p.Ile232Asn
NM_001190383.1:c.602T>A (GNE)	NP_001177312.1:p.Ile201Asn
NM_001190384.1:c.425T>A (GNE)	NP_001177313.1:p.Ile142Asn
NM_001190388.1:c.587T>A (GNE)	NP_001177317.1:p.Ile196Asn
NM_005476.5:c.602T>A (GNE)	NP_005467.1:p.Ile201Asn
XM_005251334.3:c.695T>A (GNE)	XP_005251391.1:p.Ile232Asn
NM_001190383.2:c.602T>A (GNE)	NP_001177312.1:p.Ile201Asn
NM_001190384.2:c.425T>A (GNE)	NP_001177313.1:p.Ile142Asn
NM_005476.6:c.602T>A (GNE)	NP_005467.1:p.Ile201Asn
XM_005251334.4:c.695T>A (GNE)	XP_005251391.1:p.Ile232Asn
XM_017014167.1:c.602T>A (GNE)	XP_016869656.1:p.Ile201Asn
XM_017014168.1:c.602T>A (GNE)	XP_016869657.1:p.Ile201Asn
NM_001128227.3:c.695T>A (GNE) MANE Plus Clinical	NP_001121699.1:p.Ile232Asn
NM_001190383.3:c.602T>A (GNE)	NP_001177312.1:p.Ile201Asn
NM_001190384.3:c.425T>A (GNE)	NP_001177313.1:p.Ile142Asn
NM_001190388.2:c.425T>A (GNE)	NP_001177317.2:p.Ile142Asn
NM_001374797.1:c.602T>A (GNE)	NP_001361726.1:p.Ile201Asn
NM_001374798.1:c.425T>A (GNE)	NP_001361727.1:p.Ile142Asn
NM_005476.7:c.602T>A (GNE) MANE Select	NP_005467.1:p.Ile201Asn