Canonical Allele Identifier: CA2819057138
Gene: NAGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42066358del , CM000684.2:g.42066358del GRCh38
NC_000022.10:g.42462362del , CM000684.1:g.42462362del GRCh37
NC_000022.9:g.40792308del NCBI36
NG_009247.1:g.9488del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396398.8:c.597+355del MANE Select ENSP00000379680.3:n.597+355del
ENST00000396398.7:c.597+355del ENSP00000379680.3:n.597+355del
ENST00000402937.1:c.597+355del ENSP00000384603.1:n.597+355del
ENST00000403363.5:c.597+355del ENSP00000385283.1:n.597+355del
NM_000262.2:c.597+355del NP_000253.1:n.597+355del
XM_005261615.3:c.597+355del XP_005261672.1:n.597+355del
XM_005261616.3:c.597+355del XP_005261673.1:n.597+355del
NM_001362848.1:c.597+355del NP_001349777.1:n.597+355del
NM_001362850.1:c.597+355del NP_001349779.1:n.597+355del
NM_000262.3:c.597+355del MANE Select NP_000253.1:n.597+355del