Canonical Allele Identifier: CA2406547770
Gene: NAGA HGNC NCBI

Linked Data

dbSNP Id: rs1926355521

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42061078_42061080del , CM000684.2:g.42061078_42061080del GRCh38
NC_000022.10:g.42457082_42457084del , CM000684.1:g.42457082_42457084del GRCh37
NC_000022.9:g.40787028_40787030del NCBI36
NG_009247.1:g.14765_14767del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396398.8:c.958-11_958-9del MANE Select ENSP00000379680.3:n.958-11_958-9del
ENST00000396398.7:c.958-11_958-9del ENSP00000379680.3:n.958-11_958-9del
ENST00000402937.1:c.958-11_958-9del ENSP00000384603.1:n.958-11_958-9del
ENST00000403363.5:c.958-11_958-9del ENSP00000385283.1:n.958-11_958-9del
NM_000262.2:c.958-11_958-9del NP_000253.1:n.958-11_958-9del
XM_005261615.3:c.958-11_958-9del XP_005261672.1:n.958-11_958-9del
XM_005261616.3:c.958-11_958-9del XP_005261673.1:n.958-11_958-9del
NM_001362848.1:c.958-11_958-9del NP_001349777.1:n.958-11_958-9del
NM_001362850.1:c.958-11_958-9del NP_001349779.1:n.958-11_958-9del
NM_000262.3:c.958-11_958-9del MANE Select NP_000253.1:n.958-11_958-9del