Canonical Allele Identifier: CA464494992

Gene: GNE CLTA

Linked Data

• MyVariant Identifiers: chr9:g.36219938A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36219941A>G , CM000671.2:g.36219941A>G	GRCh38
NC_000009.11:g.36219938A>G , CM000671.1:g.36219938A>G	GRCh37
NC_000009.10:g.36209938A>G	NCBI36
NG_008246.1:g.62104T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.1806T>C (GNE) MANE Plus Clinical	ENSP00000379839.3:p.Val602=
ENST00000543356.7:c.1536T>C (GNE)	ENSP00000437765.3:p.Val512=
ENST00000642385.2:c.1713T>C (GNE) MANE Select	ENSP00000494141.2:p.Val571=
ENST00000377902.5:c.1713T>C (GNE)	ENSP00000367134.4:p.Val571=
ENST00000396594.7:c.1806T>C (GNE)	ENSP00000379839.3:p.Val602=
ENST00000447283.6:c.1491T>C (GNE)	ENSP00000414760.2:p.Val497=
ENST00000464497.5:c.485+15762A>G (CLTA)	ENSP00000419158.1:n.485+15762A>G
ENST00000539208.5:c.1383T>C (GNE)	ENSP00000445117.1:p.Val461=
ENST00000539815.5:c.1713T>C (GNE)	ENSP00000439155.1:p.Val571=
ENST00000543356.6:c.1698T>C (GNE)	ENSP00000437765.2:p.Val566=
NM_001128227.2:c.1806T>C (GNE)	NP_001121699.1:p.Val602=
NM_001190383.1:c.1491T>C (GNE)	NP_001177312.1:p.Val497=
NM_001190384.1:c.1383T>C (GNE)	NP_001177313.1:p.Val461=
NM_001190388.1:c.1698T>C (GNE)	NP_001177317.1:p.Val566=
NM_005476.5:c.1713T>C (GNE)	NP_005467.1:p.Val571=
XM_005251334.3:c.1653T>C (GNE)	XP_005251391.1:p.Val551=
NM_001190383.2:c.1491T>C (GNE)	NP_001177312.1:p.Val497=
NM_001190384.2:c.1383T>C (GNE)	NP_001177313.1:p.Val461=
NM_005476.6:c.1713T>C (GNE)	NP_005467.1:p.Val571=
XM_005251334.4:c.1653T>C (GNE)	XP_005251391.1:p.Val551=
XM_017014167.1:c.1713T>C (GNE)	XP_016869656.1:p.Val571=
XM_017014168.1:c.1560T>C (GNE)	XP_016869657.1:p.Val520=
NM_001128227.3:c.1806T>C (GNE) MANE Plus Clinical	NP_001121699.1:p.Val602=
NM_001190383.3:c.1491T>C (GNE)	NP_001177312.1:p.Val497=
NM_001190384.3:c.1383T>C (GNE)	NP_001177313.1:p.Val461=
NM_001190388.2:c.1536T>C (GNE)	NP_001177317.2:p.Val512=
NM_001374797.1:c.1560T>C (GNE)	NP_001361726.1:p.Val520=
NM_001374798.1:c.1536T>C (GNE)	NP_001361727.1:p.Val512=
NM_005476.7:c.1713T>C (GNE) MANE Select	NP_005467.1:p.Val571=