Canonical Allele Identifier: CA1846324792

Gene: GNE CLTA

Linked Data

• dbSNP Id: rs1828406154

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36217947_36217960dup , CM000671.2:g.36217947_36217960dup	GRCh38
NC_000009.11:g.36217944_36217957dup , CM000671.1:g.36217944_36217957dup	GRCh37
NC_000009.10:g.36207944_36207957dup	NCBI36
NG_008246.1:g.64086_64099dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.2026+224_2026+237dup (GNE) MANE Plus Clinical	ENSP00000379839.3:n.2026+224_2026+237dup
ENST00000543356.7:c.1756+224_1756+237dup (GNE)	ENSP00000437765.3:n.1756+224_1756+237dup
ENST00000642385.2:c.1933+224_1933+237dup (GNE) MANE Select	ENSP00000494141.2:n.1933+224_1933+237dup
ENST00000377902.5:c.1933+224_1933+237dup (GNE)	ENSP00000367134.4:n.1933+224_1933+237dup
ENST00000396594.7:c.2026+224_2026+237dup (GNE)	ENSP00000379839.3:n.2026+224_2026+237dup
ENST00000447283.6:c.1711+224_1711+237dup (GNE)	ENSP00000414760.2:n.1711+224_1711+237dup
ENST00000464497.5:c.485+13768_485+13781dup (CLTA)	ENSP00000419158.1:n.485+13768_485+13781dup
ENST00000539208.5:c.1603+224_1603+237dup (GNE)	ENSP00000445117.1:n.1603+224_1603+237dup
ENST00000539815.5:c.1933+224_1933+237dup (GNE)	ENSP00000439155.1:n.1933+224_1933+237dup
ENST00000543356.6:c.1918+224_1918+237dup (GNE)	ENSP00000437765.2:n.1918+224_1918+237dup
NM_001128227.2:c.2026+224_2026+237dup (GNE)	NP_001121699.1:n.2026+224_2026+237dup
NM_001190383.1:c.1711+224_1711+237dup (GNE)	NP_001177312.1:n.1711+224_1711+237dup
NM_001190384.1:c.1603+224_1603+237dup (GNE)	NP_001177313.1:n.1603+224_1603+237dup
NM_001190388.1:c.1918+224_1918+237dup (GNE)	NP_001177317.1:n.1918+224_1918+237dup
NM_005476.5:c.1933+224_1933+237dup (GNE)	NP_005467.1:n.1933+224_1933+237dup
XM_005251334.3:c.1873+224_1873+237dup (GNE)	XP_005251391.1:n.1873+224_1873+237dup
NM_001190383.2:c.1711+224_1711+237dup (GNE)	NP_001177312.1:n.1711+224_1711+237dup
NM_001190384.2:c.1603+224_1603+237dup (GNE)	NP_001177313.1:n.1603+224_1603+237dup
NM_005476.6:c.1933+224_1933+237dup (GNE)	NP_005467.1:n.1933+224_1933+237dup
XM_005251334.4:c.1873+224_1873+237dup (GNE)	XP_005251391.1:n.1873+224_1873+237dup
XM_017014167.1:c.1933+224_1933+237dup (GNE)	XP_016869656.1:n.1933+224_1933+237dup
XM_017014168.1:c.1780+224_1780+237dup (GNE)	XP_016869657.1:n.1780+224_1780+237dup
NM_001128227.3:c.2026+224_2026+237dup (GNE) MANE Plus Clinical	NP_001121699.1:n.2026+224_2026+237dup
NM_001190383.3:c.1711+224_1711+237dup (GNE)	NP_001177312.1:n.1711+224_1711+237dup
NM_001190384.3:c.1603+224_1603+237dup (GNE)	NP_001177313.1:n.1603+224_1603+237dup
NM_001190388.2:c.1756+224_1756+237dup (GNE)	NP_001177317.2:n.1756+224_1756+237dup
NM_001374797.1:c.1780+224_1780+237dup (GNE)	NP_001361726.1:n.1780+224_1780+237dup
NM_001374798.1:c.1756+224_1756+237dup (GNE)	NP_001361727.1:n.1756+224_1756+237dup
NM_005476.7:c.1933+224_1933+237dup (GNE) MANE Select	NP_005467.1:n.1933+224_1933+237dup