Canonical Allele Identifier: CA373427132

Linked Data

dbSNP Id: rs1421444537
gnomAD v2: 9-36223384-C-T
gnomAD v4: 9-36223387-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.36223387C>T , CM000671.2:g.36223387C>T GRCh38
NC_000009.11:g.36223384C>T , CM000671.1:g.36223384C>T GRCh37
NC_000009.10:g.36213384C>T NCBI36
NG_008246.1:g.58658G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396594.8:c.1490G>A (GNE) MANE Plus Clinical ENSP00000379839.3:p.Arg497Lys
ENST00000543356.7:c.1220G>A (GNE) ENSP00000437765.3:p.Arg407Lys
ENST00000642385.2:c.1397G>A (GNE) MANE Select ENSP00000494141.2:p.Arg466Lys
ENST00000377902.5:c.1397G>A (GNE) ENSP00000367134.4:p.Arg466Lys
ENST00000396594.7:c.1490G>A (GNE) ENSP00000379839.3:p.Arg497Lys
ENST00000447283.6:c.1397G>A (GNE) ENSP00000414760.2:p.Arg466Lys
ENST00000464497.5:c.485+19208C>T (CLTA) ENSP00000419158.1:n.485+19208C>T
ENST00000539208.5:c.1067G>A (GNE) ENSP00000445117.1:p.Arg356Lys
ENST00000539815.5:c.1397G>A (GNE) ENSP00000439155.1:p.Arg466Lys
ENST00000543356.6:c.1382G>A (GNE) ENSP00000437765.2:p.Arg461Lys
NM_001128227.2:c.1490G>A (GNE) NP_001121699.1:p.Arg497Lys
NM_001190383.1:c.1397G>A (GNE) NP_001177312.1:p.Arg466Lys
NM_001190384.1:c.1067G>A (GNE) NP_001177313.1:p.Arg356Lys
NM_001190388.1:c.1382G>A (GNE) NP_001177317.1:p.Arg461Lys
NM_005476.5:c.1397G>A (GNE) NP_005467.1:p.Arg466Lys
XM_005251334.3:c.1337G>A (GNE) XP_005251391.1:p.Arg446Lys
NM_001190383.2:c.1397G>A (GNE) NP_001177312.1:p.Arg466Lys
NM_001190384.2:c.1067G>A (GNE) NP_001177313.1:p.Arg356Lys
NM_005476.6:c.1397G>A (GNE) NP_005467.1:p.Arg466Lys
XM_005251334.4:c.1337G>A (GNE) XP_005251391.1:p.Arg446Lys
XM_017014167.1:c.1397G>A (GNE) XP_016869656.1:p.Arg466Lys
XM_017014168.1:c.1244G>A (GNE) XP_016869657.1:p.Arg415Lys
NM_001128227.3:c.1490G>A (GNE) MANE Plus Clinical NP_001121699.1:p.Arg497Lys
NM_001190383.3:c.1397G>A (GNE) NP_001177312.1:p.Arg466Lys
NM_001190384.3:c.1067G>A (GNE) NP_001177313.1:p.Arg356Lys
NM_001190388.2:c.1220G>A (GNE) NP_001177317.2:p.Arg407Lys
NM_001374797.1:c.1244G>A (GNE) NP_001361726.1:p.Arg415Lys
NM_001374798.1:c.1220G>A (GNE) NP_001361727.1:p.Arg407Lys
NM_005476.7:c.1397G>A (GNE) MANE Select NP_005467.1:p.Arg466Lys