Canonical Allele Identifier: CA10263777
Gene: NAGA HGNC NCBI

Linked Data

ClinVar Variation Id: 2193002
ClinVar RCV Id: RCV002607763
dbSNP Id: rs367943149

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42066766G>A , CM000684.2:g.42066766G>A GRCh38
NC_000022.10:g.42462770G>A , CM000684.1:g.42462770G>A GRCh37
NC_000022.9:g.40792716G>A NCBI36
NG_009247.1:g.9077C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000396398.8:c.541C>T MANE Select ENSP00000379680.3:p.Arg181Cys
ENST00000396398.7:c.541C>T ENSP00000379680.3:p.Arg181Cys
ENST00000402937.1:c.541C>T ENSP00000384603.1:p.Arg181Cys
ENST00000403363.5:c.541C>T ENSP00000385283.1:p.Arg181Cys
NM_000262.2:c.541C>T NP_000253.1:p.Arg181Cys
XM_005261615.3:c.541C>T XP_005261672.1:p.Arg181Cys
XM_005261616.3:c.541C>T XP_005261673.1:p.Arg181Cys
NM_001362848.1:c.541C>T NP_001349777.1:p.Arg181Cys
NM_001362850.1:c.541C>T NP_001349779.1:p.Arg181Cys
NM_000262.3:c.541C>T MANE Select NP_000253.1:p.Arg181Cys