Canonical Allele Identifier: CA2406547676
Gene: NAGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42060878_42060879delinsGA , CM000684.2:g.42060878_42060879delinsGA GRCh38
NC_000022.10:g.42456882_42456883delinsGA , CM000684.1:g.42456882_42456883delinsGA GRCh37
NC_000022.9:g.40786828_40786829delinsGA NCBI36
NG_009247.1:g.14964_14965delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000396398.8:c.1101+45_1101+46delinsTC MANE Select ENSP00000379680.3:n.1101+45_1101+46delinsTC
ENST00000396398.7:c.1101+45_1101+46delinsTC ENSP00000379680.3:n.1101+45_1101+46delinsTC
ENST00000402937.1:c.1101+45_1101+46delinsTC ENSP00000384603.1:n.1101+45_1101+46delinsTC
ENST00000403363.5:c.1101+45_1101+46delinsTC ENSP00000385283.1:n.1101+45_1101+46delinsTC
NM_000262.2:c.1101+45_1101+46delinsTC NP_000253.1:n.1101+45_1101+46delinsTC
XM_005261615.3:c.1101+45_1101+46delinsTC XP_005261672.1:n.1101+45_1101+46delinsTC
XM_005261616.3:c.1101+45_1101+46delinsTC XP_005261673.1:n.1101+45_1101+46delinsTC
NM_001362848.1:c.1101+45_1101+46delinsTC NP_001349777.1:n.1101+45_1101+46delinsTC
NM_001362850.1:c.1101+45_1101+46delinsTC NP_001349779.1:n.1101+45_1101+46delinsTC
NM_000262.3:c.1101+45_1101+46delinsTC MANE Select NP_000253.1:n.1101+45_1101+46delinsTC