Canonical Allele Identifier: CA2406550236
Gene: NAGA HGNC NCBI

Linked Data

dbSNP Id: rs1926731260

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42066375_42066376del , CM000684.2:g.42066375_42066376del GRCh38
NC_000022.10:g.42462379_42462380del , CM000684.1:g.42462379_42462380del GRCh37
NC_000022.9:g.40792325_40792326del NCBI36
NG_009247.1:g.9468_9469del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396398.8:c.597+335_597+336del MANE Select ENSP00000379680.3:n.597+335_597+336del
ENST00000396398.7:c.597+335_597+336del ENSP00000379680.3:n.597+335_597+336del
ENST00000402937.1:c.597+335_597+336del ENSP00000384603.1:n.597+335_597+336del
ENST00000403363.5:c.597+335_597+336del ENSP00000385283.1:n.597+335_597+336del
NM_000262.2:c.597+335_597+336del NP_000253.1:n.597+335_597+336del
XM_005261615.3:c.597+335_597+336del XP_005261672.1:n.597+335_597+336del
XM_005261616.3:c.597+335_597+336del XP_005261673.1:n.597+335_597+336del
NM_001362848.1:c.597+335_597+336del NP_001349777.1:n.597+335_597+336del
NM_001362850.1:c.597+335_597+336del NP_001349779.1:n.597+335_597+336del
NM_000262.3:c.597+335_597+336del MANE Select NP_000253.1:n.597+335_597+336del