Canonical Allele Identifier: CA373425221

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.36218278C>A , CM000671.2:g.36218278C>A GRCh38
NC_000009.11:g.36218275C>A , CM000671.1:g.36218275C>A GRCh37
NC_000009.10:g.36208275C>A NCBI36
NG_008246.1:g.63767G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000396594.8:c.1931G>T (GNE) MANE Plus Clinical ENSP00000379839.3:p.Gly644Val
ENST00000543356.7:c.1661G>T (GNE) ENSP00000437765.3:p.Gly554Val
ENST00000642385.2:c.1838G>T (GNE) MANE Select ENSP00000494141.2:p.Gly613Val
ENST00000377902.5:c.1838G>T (GNE) ENSP00000367134.4:p.Gly613Val
ENST00000396594.7:c.1931G>T (GNE) ENSP00000379839.3:p.Gly644Val
ENST00000447283.6:c.1616G>T (GNE) ENSP00000414760.2:p.Gly539Val
ENST00000464497.5:c.485+14099C>A (CLTA) ENSP00000419158.1:n.485+14099C>A
ENST00000539208.5:c.1508G>T (GNE) ENSP00000445117.1:p.Gly503Val
ENST00000539815.5:c.1838G>T (GNE) ENSP00000439155.1:p.Gly613Val
ENST00000543356.6:c.1823G>T (GNE) ENSP00000437765.2:p.Gly608Val
NM_001128227.2:c.1931G>T (GNE) NP_001121699.1:p.Gly644Val
NM_001190383.1:c.1616G>T (GNE) NP_001177312.1:p.Gly539Val
NM_001190384.1:c.1508G>T (GNE) NP_001177313.1:p.Gly503Val
NM_001190388.1:c.1823G>T (GNE) NP_001177317.1:p.Gly608Val
NM_005476.5:c.1838G>T (GNE) NP_005467.1:p.Gly613Val
XM_005251334.3:c.1778G>T (GNE) XP_005251391.1:p.Gly593Val
NM_001190383.2:c.1616G>T (GNE) NP_001177312.1:p.Gly539Val
NM_001190384.2:c.1508G>T (GNE) NP_001177313.1:p.Gly503Val
NM_005476.6:c.1838G>T (GNE) NP_005467.1:p.Gly613Val
XM_005251334.4:c.1778G>T (GNE) XP_005251391.1:p.Gly593Val
XM_017014167.1:c.1838G>T (GNE) XP_016869656.1:p.Gly613Val
XM_017014168.1:c.1685G>T (GNE) XP_016869657.1:p.Gly562Val
NM_001128227.3:c.1931G>T (GNE) MANE Plus Clinical NP_001121699.1:p.Gly644Val
NM_001190383.3:c.1616G>T (GNE) NP_001177312.1:p.Gly539Val
NM_001190384.3:c.1508G>T (GNE) NP_001177313.1:p.Gly503Val
NM_001190388.2:c.1661G>T (GNE) NP_001177317.2:p.Gly554Val
NM_001374797.1:c.1685G>T (GNE) NP_001361726.1:p.Gly562Val
NM_001374798.1:c.1661G>T (GNE) NP_001361727.1:p.Gly554Val
NM_005476.7:c.1838G>T (GNE) MANE Select NP_005467.1:p.Gly613Val