Canonical Allele Identifier: CA1846375388

Gene: GNE CLTA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36246197T= , CM000671.2:g.36246197T=	GRCh38
NC_000009.11:g.36246194T= , CM000671.1:g.36246194T=	GRCh37
NC_000009.10:g.36236194T=	NCBI36
NG_008246.1:g.35848A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.543A= (GNE) MANE Plus Clinical	ENSP00000379839.3:p.Ile181=
ENST00000543356.7:c.273A= (GNE)	ENSP00000437765.3:p.Ile91=
ENST00000642385.2:c.450A= (GNE) MANE Select	ENSP00000494141.2:p.Ile150=
ENST00000377902.5:c.450A= (GNE)	ENSP00000367134.4:p.Ile150=
ENST00000396594.7:c.543A= (GNE)	ENSP00000379839.3:p.Ile181=
ENST00000447283.6:c.450A= (GNE)	ENSP00000414760.2:p.Ile150=
ENST00000464497.5:c.486-17001T= (CLTA)	ENSP00000419158.1:n.486-17001T=
ENST00000539208.5:c.273A= (GNE)	ENSP00000445117.1:p.Ile91=
ENST00000539815.5:c.450A= (GNE)	ENSP00000439155.1:p.Ile150=
ENST00000543356.6:c.435A= (GNE)	ENSP00000437765.2:p.Ile145=
NM_001128227.2:c.543A= (GNE)	NP_001121699.1:p.Ile181=
NM_001190383.1:c.450A= (GNE)	NP_001177312.1:p.Ile150=
NM_001190384.1:c.273A= (GNE)	NP_001177313.1:p.Ile91=
NM_001190388.1:c.435A= (GNE)	NP_001177317.1:p.Ile145=
NM_005476.5:c.450A= (GNE)	NP_005467.1:p.Ile150=
XM_005251334.3:c.543A= (GNE)	XP_005251391.1:p.Ile181=
NM_001190383.2:c.450A= (GNE)	NP_001177312.1:p.Ile150=
NM_001190384.2:c.273A= (GNE)	NP_001177313.1:p.Ile91=
NM_005476.6:c.450A= (GNE)	NP_005467.1:p.Ile150=
XM_005251334.4:c.543A= (GNE)	XP_005251391.1:p.Ile181=
XM_017014167.1:c.450A= (GNE)	XP_016869656.1:p.Ile150=
XM_017014168.1:c.450A= (GNE)	XP_016869657.1:p.Ile150=
NM_001128227.3:c.543A= (GNE) MANE Plus Clinical	NP_001121699.1:p.Ile181=
NM_001190383.3:c.450A= (GNE)	NP_001177312.1:p.Ile150=
NM_001190384.3:c.273A= (GNE)	NP_001177313.1:p.Ile91=
NM_001190388.2:c.273A= (GNE)	NP_001177317.2:p.Ile91=
NM_001374797.1:c.450A= (GNE)	NP_001361726.1:p.Ile150=
NM_001374798.1:c.273A= (GNE)	NP_001361727.1:p.Ile91=
NM_005476.7:c.450A= (GNE) MANE Select	NP_005467.1:p.Ile150=