Canonical Allele Identifier: CA2406548662
Gene: NAGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42063038_42063041delinsAGAG , CM000684.2:g.42063038_42063041delinsAGAG GRCh38
NC_000022.10:g.42459042_42459045delinsAGAG , CM000684.1:g.42459042_42459045delinsAGAG GRCh37
NC_000022.9:g.40788988_40788991delinsAGAG NCBI36
NG_009247.1:g.12802_12805delinsCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000396398.8:c.760-17_760-14delinsCTCT MANE Select ENSP00000379680.3:n.760-17_760-14delinsCTCT
ENST00000396398.7:c.760-17_760-14delinsCTCT ENSP00000379680.3:n.760-17_760-14delinsCTCT
ENST00000402937.1:c.760-17_760-14delinsCTCT ENSP00000384603.1:n.760-17_760-14delinsCTCT
ENST00000403363.5:c.760-17_760-14delinsCTCT ENSP00000385283.1:n.760-17_760-14delinsCTCT
NM_000262.2:c.760-17_760-14delinsCTCT NP_000253.1:n.760-17_760-14delinsCTCT
XM_005261615.3:c.760-17_760-14delinsCTCT XP_005261672.1:n.760-17_760-14delinsCTCT
XM_005261616.3:c.760-17_760-14delinsCTCT XP_005261673.1:n.760-17_760-14delinsCTCT
NM_001362848.1:c.760-17_760-14delinsCTCT NP_001349777.1:n.760-17_760-14delinsCTCT
NM_001362850.1:c.760-17_760-14delinsCTCT NP_001349779.1:n.760-17_760-14delinsCTCT
NM_000262.3:c.760-17_760-14delinsCTCT MANE Select NP_000253.1:n.760-17_760-14delinsCTCT