Canonical Allele Identifier: CA1846333239

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.36222788A= , CM000671.2:g.36222788A= GRCh38
NC_000009.11:g.36222785A= , CM000671.1:g.36222785A= GRCh37
NC_000009.10:g.36212785A= NCBI36
NG_008246.1:g.59257T=

Transcript Alleles

HGVS Amino-acid change
ENST00000396594.8:c.1715T= (GNE) MANE Plus Clinical ENSP00000379839.3:p.Ile572=
ENST00000543356.7:c.1445T= (GNE) ENSP00000437765.3:p.Ile482=
ENST00000642385.2:c.1622T= (GNE) MANE Select ENSP00000494141.2:p.Ile541=
ENST00000377902.5:c.1622T= (GNE) ENSP00000367134.4:p.Ile541=
ENST00000396594.7:c.1715T= (GNE) ENSP00000379839.3:p.Ile572=
ENST00000447283.6:c.1411+585T= (GNE) ENSP00000414760.2:n.1411+585T=
ENST00000464497.5:c.485+18609A= (CLTA) ENSP00000419158.1:n.485+18609A=
ENST00000539208.5:c.1292T= (GNE) ENSP00000445117.1:p.Ile431=
ENST00000539815.5:c.1622T= (GNE) ENSP00000439155.1:p.Ile541=
ENST00000543356.6:c.1607T= (GNE) ENSP00000437765.2:p.Ile536=
NM_001128227.2:c.1715T= (GNE) NP_001121699.1:p.Ile572=
NM_001190383.1:c.1411+585T= (GNE) NP_001177312.1:n.1411+585T=
NM_001190384.1:c.1292T= (GNE) NP_001177313.1:p.Ile431=
NM_001190388.1:c.1607T= (GNE) NP_001177317.1:p.Ile536=
NM_005476.5:c.1622T= (GNE) NP_005467.1:p.Ile541=
XM_005251334.3:c.1562T= (GNE) XP_005251391.1:p.Ile521=
NM_001190383.2:c.1411+585T= (GNE) NP_001177312.1:n.1411+585T=
NM_001190384.2:c.1292T= (GNE) NP_001177313.1:p.Ile431=
NM_005476.6:c.1622T= (GNE) NP_005467.1:p.Ile541=
XM_005251334.4:c.1562T= (GNE) XP_005251391.1:p.Ile521=
XM_017014167.1:c.1622T= (GNE) XP_016869656.1:p.Ile541=
XM_017014168.1:c.1469T= (GNE) XP_016869657.1:p.Ile490=
NM_001128227.3:c.1715T= (GNE) MANE Plus Clinical NP_001121699.1:p.Ile572=
NM_001190383.3:c.1411+585T= (GNE) NP_001177312.1:n.1411+585T=
NM_001190384.3:c.1292T= (GNE) NP_001177313.1:p.Ile431=
NM_001190388.2:c.1445T= (GNE) NP_001177317.2:p.Ile482=
NM_001374797.1:c.1469T= (GNE) NP_001361726.1:p.Ile490=
NM_001374798.1:c.1445T= (GNE) NP_001361727.1:p.Ile482=
NM_005476.7:c.1622T= (GNE) MANE Select NP_005467.1:p.Ile541=