Canonical Allele Identifier: CA464494850

Gene: GNE CLTA

Linked Data

• dbSNP Id: rs1828424112
• MyVariant Identifiers: chr9:g.36218268T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36218271T>G , CM000671.2:g.36218271T>G	GRCh38
NC_000009.11:g.36218268T>G , CM000671.1:g.36218268T>G	GRCh37
NC_000009.10:g.36208268T>G	NCBI36
NG_008246.1:g.63774A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.1938A>C (GNE) MANE Plus Clinical	ENSP00000379839.3:p.Ser646=
ENST00000543356.7:c.1668A>C (GNE)	ENSP00000437765.3:p.Ser556=
ENST00000642385.2:c.1845A>C (GNE) MANE Select	ENSP00000494141.2:p.Ser615=
ENST00000377902.5:c.1845A>C (GNE)	ENSP00000367134.4:p.Ser615=
ENST00000396594.7:c.1938A>C (GNE)	ENSP00000379839.3:p.Ser646=
ENST00000447283.6:c.1623A>C (GNE)	ENSP00000414760.2:p.Ser541=
ENST00000464497.5:c.485+14092T>G (CLTA)	ENSP00000419158.1:n.485+14092T>G
ENST00000539208.5:c.1515A>C (GNE)	ENSP00000445117.1:p.Ser505=
ENST00000539815.5:c.1845A>C (GNE)	ENSP00000439155.1:p.Ser615=
ENST00000543356.6:c.1830A>C (GNE)	ENSP00000437765.2:p.Ser610=
NM_001128227.2:c.1938A>C (GNE)	NP_001121699.1:p.Ser646=
NM_001190383.1:c.1623A>C (GNE)	NP_001177312.1:p.Ser541=
NM_001190384.1:c.1515A>C (GNE)	NP_001177313.1:p.Ser505=
NM_001190388.1:c.1830A>C (GNE)	NP_001177317.1:p.Ser610=
NM_005476.5:c.1845A>C (GNE)	NP_005467.1:p.Ser615=
XM_005251334.3:c.1785A>C (GNE)	XP_005251391.1:p.Ser595=
NM_001190383.2:c.1623A>C (GNE)	NP_001177312.1:p.Ser541=
NM_001190384.2:c.1515A>C (GNE)	NP_001177313.1:p.Ser505=
NM_005476.6:c.1845A>C (GNE)	NP_005467.1:p.Ser615=
XM_005251334.4:c.1785A>C (GNE)	XP_005251391.1:p.Ser595=
XM_017014167.1:c.1845A>C (GNE)	XP_016869656.1:p.Ser615=
XM_017014168.1:c.1692A>C (GNE)	XP_016869657.1:p.Ser564=
NM_001128227.3:c.1938A>C (GNE) MANE Plus Clinical	NP_001121699.1:p.Ser646=
NM_001190383.3:c.1623A>C (GNE)	NP_001177312.1:p.Ser541=
NM_001190384.3:c.1515A>C (GNE)	NP_001177313.1:p.Ser505=
NM_001190388.2:c.1668A>C (GNE)	NP_001177317.2:p.Ser556=
NM_001374797.1:c.1692A>C (GNE)	NP_001361726.1:p.Ser564=
NM_001374798.1:c.1668A>C (GNE)	NP_001361727.1:p.Ser556=
NM_005476.7:c.1845A>C (GNE) MANE Select	NP_005467.1:p.Ser615=