Canonical Allele Identifier: CA241583

Linked Data

ClinVar Variation Id: 195244
dbSNP Id: rs794727279
gnomAD v2: 9-36249367-G-A
gnomAD v4: 9-36249370-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.36249370G>A , CM000671.2:g.36249370G>A GRCh38
NC_000009.11:g.36249367G>A , CM000671.1:g.36249367G>A GRCh37
NC_000009.10:g.36239367G>A NCBI36
NG_008246.1:g.32675C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000396594.8:c.79C>T (GNE) MANE Plus Clinical ENSP00000379839.3:p.Arg27Ter
ENST00000543356.7:c.-13-2888C>T (GNE) ENSP00000437765.3:n.-13-2888C>T
ENST00000642385.2:c.-15C>T (GNE) MANE Select ENSP00000494141.2:n.-15C>T
ENST00000377902.5:c.-15C>T (GNE) ENSP00000367134.4:n.-15C>T
ENST00000396594.7:c.79C>T (GNE) ENSP00000379839.3:p.Arg27Ter
ENST00000447283.6:c.-15C>T (GNE) ENSP00000414760.2:n.-15C>T
ENST00000464497.5:c.486-13828G>A (CLTA) ENSP00000419158.1:n.486-13828G>A
ENST00000539208.5:c.-13-2888C>T (GNE) ENSP00000445117.1:n.-13-2888C>T
ENST00000539815.5:c.-15C>T (GNE) ENSP00000439155.1:n.-15C>T
ENST00000543356.6:c.150-2888C>T (GNE) ENSP00000437765.2:n.150-2888C>T
NM_001128227.2:c.79C>T (GNE) NP_001121699.1:p.Arg27Ter
NM_001190383.1:c.-15C>T (GNE) NP_001177312.1:n.-15C>T
NM_001190384.1:c.-13-2888C>T (GNE) NP_001177313.1:n.-13-2888C>T
NM_001190388.1:c.150-2888C>T (GNE) NP_001177317.1:n.150-2888C>T
NM_005476.5:c.-15C>T (GNE) NP_005467.1:n.-15C>T
XM_005251334.3:c.79C>T (GNE) XP_005251391.1:p.Arg27Ter
NM_001190383.2:c.-15C>T (GNE) NP_001177312.1:n.-15C>T
NM_001190384.2:c.-13-2888C>T (GNE) NP_001177313.1:n.-13-2888C>T
NM_005476.6:c.-15C>T (GNE) NP_005467.1:n.-15C>T
XM_005251334.4:c.79C>T (GNE) XP_005251391.1:p.Arg27Ter
XM_017014167.1:c.-15C>T (GNE) XP_016869656.1:n.-15C>T
XM_017014168.1:c.-15C>T (GNE) XP_016869657.1:n.-15C>T
NM_001128227.3:c.79C>T (GNE) MANE Plus Clinical NP_001121699.1:p.Arg27Ter
NM_001190383.3:c.-15C>T (GNE) NP_001177312.1:n.-15C>T
NM_001190384.3:c.-13-2888C>T (GNE) NP_001177313.1:n.-13-2888C>T
NM_001190388.2:c.-13-2888C>T (GNE) NP_001177317.2:n.-13-2888C>T
NM_001374797.1:c.-15C>T (GNE) NP_001361726.1:n.-15C>T
NM_001374798.1:c.-13-2888C>T (GNE) NP_001361727.1:n.-13-2888C>T
NM_005476.7:c.-15C>T (GNE) MANE Select NP_005467.1:n.-15C>T