Canonical Allele Identifier: CA2988346722
Gene: NAGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42062936del , CM000684.2:g.42062936del GRCh38
NC_000022.10:g.42458940del , CM000684.1:g.42458940del GRCh37
NC_000022.9:g.40788886del NCBI36
NG_009247.1:g.12908del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396398.8:c.849del MANE Select ENSP00000379680.3:p.Thr284GlnfsTer19
ENST00000396398.7:c.849del ENSP00000379680.3:p.Thr284GlnfsTer19
ENST00000402937.1:c.849del ENSP00000384603.1:p.Thr284GlnfsTer19
ENST00000403363.5:c.849del ENSP00000385283.1:p.Thr284GlnfsTer19
NM_000262.2:c.849del NP_000253.1:p.Thr284GlnfsTer19
XM_005261615.3:c.849del XP_005261672.1:p.Thr284GlnfsTer19
XM_005261616.3:c.849del XP_005261673.1:p.Thr284GlnfsTer19
NM_001362848.1:c.849del NP_001349777.1:p.Thr284GlnfsTer19
NM_001362850.1:c.849del NP_001349779.1:p.Thr284GlnfsTer19
NM_000262.3:c.849del MANE Select NP_000253.1:p.Thr284GlnfsTer19