Canonical Allele Identifier: CA1846333211

Gene: GNE CLTA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.36222773_36222777delinsTTACC , CM000671.2:g.36222773_36222777delinsTTACC	GRCh38
NC_000009.11:g.36222770_36222774delinsTTACC , CM000671.1:g.36222770_36222774delinsTTACC	GRCh37
NC_000009.10:g.36212770_36212774delinsTTACC	NCBI36
NG_008246.1:g.59268_59272delinsGGTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396594.8:c.1726_1726+4delinsGGTAA (GNE)
ENST00000543356.7:c.1456_1456+4delinsGGTAA (GNE)
ENST00000642385.2:c.1633_1633+4delinsGGTAA (GNE)
ENST00000377902.5:c.1633_1633+4delinsGGTAA (GNE)
ENST00000396594.7:c.1726_1726+4delinsGGTAA (GNE)
ENST00000447283.6:c.1411+596_1411+600delinsGGTAA (GNE)	ENSP00000414760.2:n.1411+596_1411+600delinsGGTAA
ENST00000464497.5:c.485+18594_485+18598delinsTTACC (CLTA)	ENSP00000419158.1:n.485+18594_485+18598delinsTTACC
ENST00000539208.5:c.1303_1303+4delinsGGTAA (GNE)
ENST00000539815.5:c.1633_1633+4delinsGGTAA (GNE)
ENST00000543356.6:c.1618_1618+4delinsGGTAA (GNE)
NM_001128227.2:c.1726_1726+4delinsGGTAA (GNE)
NM_001190383.1:c.1411+596_1411+600delinsGGTAA (GNE)	NP_001177312.1:n.1411+596_1411+600delinsGGTAA
NM_001190384.1:c.1303_1303+4delinsGGTAA (GNE)
NM_001190388.1:c.1618_1618+4delinsGGTAA (GNE)
NM_005476.5:c.1633_1633+4delinsGGTAA (GNE)
XM_005251334.3:c.1573_1573+4delinsGGTAA (GNE)
NM_001190383.2:c.1411+596_1411+600delinsGGTAA (GNE)	NP_001177312.1:n.1411+596_1411+600delinsGGTAA
NM_001190384.2:c.1303_1303+4delinsGGTAA (GNE)
NM_005476.6:c.1633_1633+4delinsGGTAA (GNE)
XM_005251334.4:c.1573_1573+4delinsGGTAA (GNE)
XM_017014167.1:c.1633_1633+4delinsGGTAA (GNE)
XM_017014168.1:c.1480_1480+4delinsGGTAA (GNE)
NM_001128227.3:c.1726_1726+4delinsGGTAA (GNE)
NM_001190383.3:c.1411+596_1411+600delinsGGTAA (GNE)	NP_001177312.1:n.1411+596_1411+600delinsGGTAA
NM_001190384.3:c.1303_1303+4delinsGGTAA (GNE)
NM_001190388.2:c.1456_1456+4delinsGGTAA (GNE)
NM_001374797.1:c.1480_1480+4delinsGGTAA (GNE)
NM_001374798.1:c.1456_1456+4delinsGGTAA (GNE)
NM_005476.7:c.1633_1633+4delinsGGTAA (GNE)