Canonical Allele Identifier: CA192841494

Gene: GNE CLTA

Linked Data

• ClinVar Variation Id: 2194184
• ClinVar RCV Id: RCV002612441
• dbSNP Id: rs980752867
• gnomAD v4: 9-36220031-G-A
• MyVariant Identifiers: chr9:g.36220028G>A (hg19) ; chr9:g.36220031G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36220031G>A , CM000671.2:g.36220031G>A	GRCh38
NC_000009.11:g.36220028G>A , CM000671.1:g.36220028G>A	GRCh37
NC_000009.10:g.36210028G>A	NCBI36
NG_008246.1:g.62014C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.1727-11C>T (GNE) MANE Plus Clinical	ENSP00000379839.3:n.1727-11C>T
ENST00000543356.7:c.1457-11C>T (GNE)	ENSP00000437765.3:n.1457-11C>T
ENST00000642385.2:c.1634-11C>T (GNE) MANE Select	ENSP00000494141.2:n.1634-11C>T
ENST00000377902.5:c.1634-11C>T (GNE)	ENSP00000367134.4:n.1634-11C>T
ENST00000396594.7:c.1727-11C>T (GNE)	ENSP00000379839.3:n.1727-11C>T
ENST00000447283.6:c.1412-11C>T (GNE)	ENSP00000414760.2:n.1412-11C>T
ENST00000464497.5:c.485+15852G>A (CLTA)	ENSP00000419158.1:n.485+15852G>A
ENST00000539208.5:c.1304-11C>T (GNE)	ENSP00000445117.1:n.1304-11C>T
ENST00000539815.5:c.1634-11C>T (GNE)	ENSP00000439155.1:n.1634-11C>T
ENST00000543356.6:c.1619-11C>T (GNE)	ENSP00000437765.2:n.1619-11C>T
NM_001128227.2:c.1727-11C>T (GNE)	NP_001121699.1:n.1727-11C>T
NM_001190383.1:c.1412-11C>T (GNE)	NP_001177312.1:n.1412-11C>T
NM_001190384.1:c.1304-11C>T (GNE)	NP_001177313.1:n.1304-11C>T
NM_001190388.1:c.1619-11C>T (GNE)	NP_001177317.1:n.1619-11C>T
NM_005476.5:c.1634-11C>T (GNE)	NP_005467.1:n.1634-11C>T
XM_005251334.3:c.1574-11C>T (GNE)	XP_005251391.1:n.1574-11C>T
NM_001190383.2:c.1412-11C>T (GNE)	NP_001177312.1:n.1412-11C>T
NM_001190384.2:c.1304-11C>T (GNE)	NP_001177313.1:n.1304-11C>T
NM_005476.6:c.1634-11C>T (GNE)	NP_005467.1:n.1634-11C>T
XM_005251334.4:c.1574-11C>T (GNE)	XP_005251391.1:n.1574-11C>T
XM_017014167.1:c.1634-11C>T (GNE)	XP_016869656.1:n.1634-11C>T
XM_017014168.1:c.1481-11C>T (GNE)	XP_016869657.1:n.1481-11C>T
NM_001128227.3:c.1727-11C>T (GNE) MANE Plus Clinical	NP_001121699.1:n.1727-11C>T
NM_001190383.3:c.1412-11C>T (GNE)	NP_001177312.1:n.1412-11C>T
NM_001190384.3:c.1304-11C>T (GNE)	NP_001177313.1:n.1304-11C>T
NM_001190388.2:c.1457-11C>T (GNE)	NP_001177317.2:n.1457-11C>T
NM_001374797.1:c.1481-11C>T (GNE)	NP_001361726.1:n.1481-11C>T
NM_001374798.1:c.1457-11C>T (GNE)	NP_001361727.1:n.1457-11C>T
NM_005476.7:c.1634-11C>T (GNE) MANE Select	NP_005467.1:n.1634-11C>T