Canonical Allele Identifier: CA373430824
Community Standard Title: NM_005476.7(GNE):c.811G>T (p.Glu271Ter)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.36234091C>A , CM000671.2:g.36234091C>A GRCh38
NC_000009.11:g.36234088C>A , CM000671.1:g.36234088C>A GRCh37
NC_000009.10:g.36224088C>A NCBI36
NG_008246.1:g.47954G>T

Transcript Alleles

HGVS Amino-acid Change
NM_005476.7:c.811G>T (GNE) MANE Select NP_005467.1:p.Glu271Ter
ENST00000642385.2:c.811G>T (GNE) MANE Select ENSP00000494141.2:p.Glu271Ter
NM_001128227.3:c.904G>T (GNE) MANE Plus Clinical NP_001121699.1:p.Glu302Ter
ENST00000396594.8:c.904G>T (GNE) MANE Plus Clinical ENSP00000379839.3:p.Glu302Ter
NM_001128227.2:c.904G>T (GNE) NP_001121699.1:p.Glu302Ter
NM_001190383.1:c.811G>T (GNE) NP_001177312.1:p.Glu271Ter
NM_001190383.2:c.811G>T (GNE) NP_001177312.1:p.Glu271Ter
NM_001190383.3:c.811G>T (GNE) NP_001177312.1:p.Glu271Ter
NM_001190384.1:c.481G>T (GNE) NP_001177313.1:p.Glu161Ter
NM_001190384.2:c.481G>T (GNE) NP_001177313.1:p.Glu161Ter
NM_001190384.3:c.481G>T (GNE) NP_001177313.1:p.Glu161Ter
NM_001190388.1:c.796G>T (GNE) NP_001177317.1:p.Glu266Ter
NM_001190388.2:c.634G>T (GNE) NP_001177317.2:p.Glu212Ter
NM_001374797.1:c.658G>T (GNE) NP_001361726.1:p.Glu220Ter
NM_001374798.1:c.634G>T (GNE) NP_001361727.1:p.Glu212Ter
NM_005476.5:c.811G>T (GNE) NP_005467.1:p.Glu271Ter
NM_005476.6:c.811G>T (GNE) NP_005467.1:p.Glu271Ter
ENST00000377902.5:c.811G>T (GNE) ENSP00000367134.4:p.Glu271Ter
ENST00000396594.7:c.904G>T (GNE) ENSP00000379839.3:p.Glu302Ter
ENST00000447283.6:c.811G>T (GNE) ENSP00000414760.2:p.Glu271Ter
ENST00000464497.5:c.486-29107C>A (CLTA) ENSP00000419158.1:n.486-29107C>A
ENST00000539208.5:c.481G>T (GNE) ENSP00000445117.1:p.Glu161Ter
ENST00000539815.5:c.811G>T (GNE) ENSP00000439155.1:p.Glu271Ter
ENST00000543356.6:c.796G>T (GNE) ENSP00000437765.2:p.Glu266Ter
ENST00000543356.7:c.634G>T (GNE) ENSP00000437765.3:p.Glu212Ter
XM_005251334.3:c.751G>T (GNE) XP_005251391.1:p.Glu251Ter
XM_005251334.4:c.751G>T (GNE) XP_005251391.1:p.Glu251Ter
XM_017014167.1:c.811G>T (GNE) XP_016869656.1:p.Glu271Ter
XM_017014168.1:c.658G>T (GNE) XP_016869657.1:p.Glu220Ter