Canonical Allele Identifier: CA373424963

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.36218201G>T , CM000671.2:g.36218201G>T GRCh38
NC_000009.11:g.36218198G>T , CM000671.1:g.36218198G>T GRCh37
NC_000009.10:g.36208198G>T NCBI36
NG_008246.1:g.63844C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396594.8:c.2008C>A (GNE) MANE Plus Clinical ENSP00000379839.3:p.Gln670Lys
ENST00000543356.7:c.1738C>A (GNE) ENSP00000437765.3:p.Gln580Lys
ENST00000642385.2:c.1915C>A (GNE) MANE Select ENSP00000494141.2:p.Gln639Lys
ENST00000377902.5:c.1915C>A (GNE) ENSP00000367134.4:p.Gln639Lys
ENST00000396594.7:c.2008C>A (GNE) ENSP00000379839.3:p.Gln670Lys
ENST00000447283.6:c.1693C>A (GNE) ENSP00000414760.2:p.Gln565Lys
ENST00000464497.5:c.485+14022G>T (CLTA) ENSP00000419158.1:n.485+14022G>T
ENST00000539208.5:c.1585C>A (GNE) ENSP00000445117.1:p.Gln529Lys
ENST00000539815.5:c.1915C>A (GNE) ENSP00000439155.1:p.Gln639Lys
ENST00000543356.6:c.1900C>A (GNE) ENSP00000437765.2:p.Gln634Lys
NM_001128227.2:c.2008C>A (GNE) NP_001121699.1:p.Gln670Lys
NM_001190383.1:c.1693C>A (GNE) NP_001177312.1:p.Gln565Lys
NM_001190384.1:c.1585C>A (GNE) NP_001177313.1:p.Gln529Lys
NM_001190388.1:c.1900C>A (GNE) NP_001177317.1:p.Gln634Lys
NM_005476.5:c.1915C>A (GNE) NP_005467.1:p.Gln639Lys
XM_005251334.3:c.1855C>A (GNE) XP_005251391.1:p.Gln619Lys
NM_001190383.2:c.1693C>A (GNE) NP_001177312.1:p.Gln565Lys
NM_001190384.2:c.1585C>A (GNE) NP_001177313.1:p.Gln529Lys
NM_005476.6:c.1915C>A (GNE) NP_005467.1:p.Gln639Lys
XM_005251334.4:c.1855C>A (GNE) XP_005251391.1:p.Gln619Lys
XM_017014167.1:c.1915C>A (GNE) XP_016869656.1:p.Gln639Lys
XM_017014168.1:c.1762C>A (GNE) XP_016869657.1:p.Gln588Lys
NM_001128227.3:c.2008C>A (GNE) MANE Plus Clinical NP_001121699.1:p.Gln670Lys
NM_001190383.3:c.1693C>A (GNE) NP_001177312.1:p.Gln565Lys
NM_001190384.3:c.1585C>A (GNE) NP_001177313.1:p.Gln529Lys
NM_001190388.2:c.1738C>A (GNE) NP_001177317.2:p.Gln580Lys
NM_001374797.1:c.1762C>A (GNE) NP_001361726.1:p.Gln588Lys
NM_001374798.1:c.1738C>A (GNE) NP_001361727.1:p.Gln580Lys
NM_005476.7:c.1915C>A (GNE) MANE Select NP_005467.1:p.Gln639Lys