Canonical Allele Identifier: CA373426760

Gene: GNE CLTA

Linked Data

• ClinVar Variation Id: 2941761
• ClinVar RCV Id: RCV003802783
• MyVariant Identifiers: chr9:g.36222941G>A (hg19) ; chr9:g.36222944G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36222944G>A , CM000671.2:g.36222944G>A	GRCh38
NC_000009.11:g.36222941G>A , CM000671.1:g.36222941G>A	GRCh37
NC_000009.10:g.36212941G>A	NCBI36
NG_008246.1:g.59101C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.1559C>T (GNE) MANE Plus Clinical	ENSP00000379839.3:p.Thr520Ile
ENST00000543356.7:c.1289C>T (GNE)	ENSP00000437765.3:p.Thr430Ile
ENST00000642385.2:c.1466C>T (GNE) MANE Select	ENSP00000494141.2:p.Thr489Ile
ENST00000377902.5:c.1466C>T (GNE)	ENSP00000367134.4:p.Thr489Ile
ENST00000396594.7:c.1559C>T (GNE)	ENSP00000379839.3:p.Thr520Ile
ENST00000447283.6:c.1411+429C>T (GNE)	ENSP00000414760.2:n.1411+429C>T
ENST00000464497.5:c.485+18765G>A (CLTA)	ENSP00000419158.1:n.485+18765G>A
ENST00000539208.5:c.1136C>T (GNE)	ENSP00000445117.1:p.Thr379Ile
ENST00000539815.5:c.1466C>T (GNE)	ENSP00000439155.1:p.Thr489Ile
ENST00000543356.6:c.1451C>T (GNE)	ENSP00000437765.2:p.Thr484Ile
NM_001128227.2:c.1559C>T (GNE)	NP_001121699.1:p.Thr520Ile
NM_001190383.1:c.1411+429C>T (GNE)	NP_001177312.1:n.1411+429C>T
NM_001190384.1:c.1136C>T (GNE)	NP_001177313.1:p.Thr379Ile
NM_001190388.1:c.1451C>T (GNE)	NP_001177317.1:p.Thr484Ile
NM_005476.5:c.1466C>T (GNE)	NP_005467.1:p.Thr489Ile
XM_005251334.3:c.1406C>T (GNE)	XP_005251391.1:p.Thr469Ile
NM_001190383.2:c.1411+429C>T (GNE)	NP_001177312.1:n.1411+429C>T
NM_001190384.2:c.1136C>T (GNE)	NP_001177313.1:p.Thr379Ile
NM_005476.6:c.1466C>T (GNE)	NP_005467.1:p.Thr489Ile
XM_005251334.4:c.1406C>T (GNE)	XP_005251391.1:p.Thr469Ile
XM_017014167.1:c.1466C>T (GNE)	XP_016869656.1:p.Thr489Ile
XM_017014168.1:c.1313C>T (GNE)	XP_016869657.1:p.Thr438Ile
NM_001128227.3:c.1559C>T (GNE) MANE Plus Clinical	NP_001121699.1:p.Thr520Ile
NM_001190383.3:c.1411+429C>T (GNE)	NP_001177312.1:n.1411+429C>T
NM_001190384.3:c.1136C>T (GNE)	NP_001177313.1:p.Thr379Ile
NM_001190388.2:c.1289C>T (GNE)	NP_001177317.2:p.Thr430Ile
NM_001374797.1:c.1313C>T (GNE)	NP_001361726.1:p.Thr438Ile
NM_001374798.1:c.1289C>T (GNE)	NP_001361727.1:p.Thr430Ile
NM_005476.7:c.1466C>T (GNE) MANE Select	NP_005467.1:p.Thr489Ile