Canonical Allele Identifier: CA373425006

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.36218213T>C , CM000671.2:g.36218213T>C GRCh38
NC_000009.11:g.36218210T>C , CM000671.1:g.36218210T>C GRCh37
NC_000009.10:g.36208210T>C NCBI36
NG_008246.1:g.63832A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396594.8:c.1996A>G (GNE) MANE Plus Clinical ENSP00000379839.3:p.Asn666Asp
ENST00000543356.7:c.1726A>G (GNE) ENSP00000437765.3:p.Asn576Asp
ENST00000642385.2:c.1903A>G (GNE) MANE Select ENSP00000494141.2:p.Asn635Asp
ENST00000377902.5:c.1903A>G (GNE) ENSP00000367134.4:p.Asn635Asp
ENST00000396594.7:c.1996A>G (GNE) ENSP00000379839.3:p.Asn666Asp
ENST00000447283.6:c.1681A>G (GNE) ENSP00000414760.2:p.Asn561Asp
ENST00000464497.5:c.485+14034T>C (CLTA) ENSP00000419158.1:n.485+14034T>C
ENST00000539208.5:c.1573A>G (GNE) ENSP00000445117.1:p.Asn525Asp
ENST00000539815.5:c.1903A>G (GNE) ENSP00000439155.1:p.Asn635Asp
ENST00000543356.6:c.1888A>G (GNE) ENSP00000437765.2:p.Asn630Asp
NM_001128227.2:c.1996A>G (GNE) NP_001121699.1:p.Asn666Asp
NM_001190383.1:c.1681A>G (GNE) NP_001177312.1:p.Asn561Asp
NM_001190384.1:c.1573A>G (GNE) NP_001177313.1:p.Asn525Asp
NM_001190388.1:c.1888A>G (GNE) NP_001177317.1:p.Asn630Asp
NM_005476.5:c.1903A>G (GNE) NP_005467.1:p.Asn635Asp
XM_005251334.3:c.1843A>G (GNE) XP_005251391.1:p.Asn615Asp
NM_001190383.2:c.1681A>G (GNE) NP_001177312.1:p.Asn561Asp
NM_001190384.2:c.1573A>G (GNE) NP_001177313.1:p.Asn525Asp
NM_005476.6:c.1903A>G (GNE) NP_005467.1:p.Asn635Asp
XM_005251334.4:c.1843A>G (GNE) XP_005251391.1:p.Asn615Asp
XM_017014167.1:c.1903A>G (GNE) XP_016869656.1:p.Asn635Asp
XM_017014168.1:c.1750A>G (GNE) XP_016869657.1:p.Asn584Asp
NM_001128227.3:c.1996A>G (GNE) MANE Plus Clinical NP_001121699.1:p.Asn666Asp
NM_001190383.3:c.1681A>G (GNE) NP_001177312.1:p.Asn561Asp
NM_001190384.3:c.1573A>G (GNE) NP_001177313.1:p.Asn525Asp
NM_001190388.2:c.1726A>G (GNE) NP_001177317.2:p.Asn576Asp
NM_001374797.1:c.1750A>G (GNE) NP_001361726.1:p.Asn584Asp
NM_001374798.1:c.1726A>G (GNE) NP_001361727.1:p.Asn576Asp
NM_005476.7:c.1903A>G (GNE) MANE Select NP_005467.1:p.Asn635Asp