Canonical Allele Identifier: CA373426619

Gene: GNE CLTA

Linked Data

• dbSNP Id: rs1828670090
• gnomAD v3: 9-36222915-C-A
• gnomAD v4: 9-36222915-C-A
• MyVariant Identifiers: chr9:g.36222912C>A (hg19) ; chr9:g.36222915C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36222915C>A , CM000671.2:g.36222915C>A	GRCh38
NC_000009.11:g.36222912C>A , CM000671.1:g.36222912C>A	GRCh37
NC_000009.10:g.36212912C>A	NCBI36
NG_008246.1:g.59130G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.1588G>T (GNE) MANE Plus Clinical	ENSP00000379839.3:p.Asp530Tyr
ENST00000543356.7:c.1318G>T (GNE)	ENSP00000437765.3:p.Asp440Tyr
ENST00000642385.2:c.1495G>T (GNE) MANE Select	ENSP00000494141.2:p.Asp499Tyr
ENST00000377902.5:c.1495G>T (GNE)	ENSP00000367134.4:p.Asp499Tyr
ENST00000396594.7:c.1588G>T (GNE)	ENSP00000379839.3:p.Asp530Tyr
ENST00000447283.6:c.1411+458G>T (GNE)	ENSP00000414760.2:n.1411+458G>T
ENST00000464497.5:c.485+18736C>A (CLTA)	ENSP00000419158.1:n.485+18736C>A
ENST00000539208.5:c.1165G>T (GNE)	ENSP00000445117.1:p.Asp389Tyr
ENST00000539815.5:c.1495G>T (GNE)	ENSP00000439155.1:p.Asp499Tyr
ENST00000543356.6:c.1480G>T (GNE)	ENSP00000437765.2:p.Asp494Tyr
NM_001128227.2:c.1588G>T (GNE)	NP_001121699.1:p.Asp530Tyr
NM_001190383.1:c.1411+458G>T (GNE)	NP_001177312.1:n.1411+458G>T
NM_001190384.1:c.1165G>T (GNE)	NP_001177313.1:p.Asp389Tyr
NM_001190388.1:c.1480G>T (GNE)	NP_001177317.1:p.Asp494Tyr
NM_005476.5:c.1495G>T (GNE)	NP_005467.1:p.Asp499Tyr
XM_005251334.3:c.1435G>T (GNE)	XP_005251391.1:p.Asp479Tyr
NM_001190383.2:c.1411+458G>T (GNE)	NP_001177312.1:n.1411+458G>T
NM_001190384.2:c.1165G>T (GNE)	NP_001177313.1:p.Asp389Tyr
NM_005476.6:c.1495G>T (GNE)	NP_005467.1:p.Asp499Tyr
XM_005251334.4:c.1435G>T (GNE)	XP_005251391.1:p.Asp479Tyr
XM_017014167.1:c.1495G>T (GNE)	XP_016869656.1:p.Asp499Tyr
XM_017014168.1:c.1342G>T (GNE)	XP_016869657.1:p.Asp448Tyr
NM_001128227.3:c.1588G>T (GNE) MANE Plus Clinical	NP_001121699.1:p.Asp530Tyr
NM_001190383.3:c.1411+458G>T (GNE)	NP_001177312.1:n.1411+458G>T
NM_001190384.3:c.1165G>T (GNE)	NP_001177313.1:p.Asp389Tyr
NM_001190388.2:c.1318G>T (GNE)	NP_001177317.2:p.Asp440Tyr
NM_001374797.1:c.1342G>T (GNE)	NP_001361726.1:p.Asp448Tyr
NM_001374798.1:c.1318G>T (GNE)	NP_001361727.1:p.Asp440Tyr
NM_005476.7:c.1495G>T (GNE) MANE Select	NP_005467.1:p.Asp499Tyr