Canonical Allele Identifier: CA192843496

Gene: GNE CLTA

Linked Data

• ClinVar Variation Id: 497075
• ClinVar RCV Id: RCV000596934 ; RCV000671522 ; RCV001378882
• dbSNP Id: rs986773986
• gnomAD v2: 9-36222824-A-C
• gnomAD v4: 9-36222827-A-C
• MyVariant Identifiers: chr9:g.36222824A>C (hg19) ; chr9:g.36222827A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36222827A>C , CM000671.2:g.36222827A>C	GRCh38
NC_000009.11:g.36222824A>C , CM000671.1:g.36222824A>C	GRCh37
NC_000009.10:g.36212824A>C	NCBI36
NG_008246.1:g.59218T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.1676T>G (GNE) MANE Plus Clinical	ENSP00000379839.3:p.Phe559Cys
ENST00000543356.7:c.1406T>G (GNE)	ENSP00000437765.3:p.Phe469Cys
ENST00000642385.2:c.1583T>G (GNE) MANE Select	ENSP00000494141.2:p.Phe528Cys
ENST00000377902.5:c.1583T>G (GNE)	ENSP00000367134.4:p.Phe528Cys
ENST00000396594.7:c.1676T>G (GNE)	ENSP00000379839.3:p.Phe559Cys
ENST00000447283.6:c.1411+546T>G (GNE)	ENSP00000414760.2:n.1411+546T>G
ENST00000464497.5:c.485+18648A>C (CLTA)	ENSP00000419158.1:n.485+18648A>C
ENST00000539208.5:c.1253T>G (GNE)	ENSP00000445117.1:p.Phe418Cys
ENST00000539815.5:c.1583T>G (GNE)	ENSP00000439155.1:p.Phe528Cys
ENST00000543356.6:c.1568T>G (GNE)	ENSP00000437765.2:p.Phe523Cys
NM_001128227.2:c.1676T>G (GNE)	NP_001121699.1:p.Phe559Cys
NM_001190383.1:c.1411+546T>G (GNE)	NP_001177312.1:n.1411+546T>G
NM_001190384.1:c.1253T>G (GNE)	NP_001177313.1:p.Phe418Cys
NM_001190388.1:c.1568T>G (GNE)	NP_001177317.1:p.Phe523Cys
NM_005476.5:c.1583T>G (GNE)	NP_005467.1:p.Phe528Cys
XM_005251334.3:c.1523T>G (GNE)	XP_005251391.1:p.Phe508Cys
NM_001190383.2:c.1411+546T>G (GNE)	NP_001177312.1:n.1411+546T>G
NM_001190384.2:c.1253T>G (GNE)	NP_001177313.1:p.Phe418Cys
NM_005476.6:c.1583T>G (GNE)	NP_005467.1:p.Phe528Cys
XM_005251334.4:c.1523T>G (GNE)	XP_005251391.1:p.Phe508Cys
XM_017014167.1:c.1583T>G (GNE)	XP_016869656.1:p.Phe528Cys
XM_017014168.1:c.1430T>G (GNE)	XP_016869657.1:p.Phe477Cys
NM_001128227.3:c.1676T>G (GNE) MANE Plus Clinical	NP_001121699.1:p.Phe559Cys
NM_001190383.3:c.1411+546T>G (GNE)	NP_001177312.1:n.1411+546T>G
NM_001190384.3:c.1253T>G (GNE)	NP_001177313.1:p.Phe418Cys
NM_001190388.2:c.1406T>G (GNE)	NP_001177317.2:p.Phe469Cys
NM_001374797.1:c.1430T>G (GNE)	NP_001361726.1:p.Phe477Cys
NM_001374798.1:c.1406T>G (GNE)	NP_001361727.1:p.Phe469Cys
NM_005476.7:c.1583T>G (GNE) MANE Select	NP_005467.1:p.Phe528Cys