Canonical Allele Identifier: CA10263728
Gene: NAGA HGNC NCBI

Linked Data

ClinVar Variation Id: 341909
dbSNP Id: rs781499383

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42065859C>T , CM000684.2:g.42065859C>T GRCh38
NC_000022.10:g.42461863C>T , CM000684.1:g.42461863C>T GRCh37
NC_000022.9:g.40791809C>T NCBI36
NG_009247.1:g.9984G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396398.8:c.638G>A MANE Select ENSP00000379680.3:p.Arg213His
ENST00000396398.7:c.638G>A ENSP00000379680.3:p.Arg213His
ENST00000402937.1:c.638G>A ENSP00000384603.1:p.Arg213His
ENST00000403363.5:c.638G>A ENSP00000385283.1:p.Arg213His
NM_000262.2:c.638G>A NP_000253.1:p.Arg213His
XM_005261615.3:c.638G>A XP_005261672.1:p.Arg213His
XM_005261616.3:c.638G>A XP_005261673.1:p.Arg213His
NM_001362848.1:c.638G>A NP_001349777.1:p.Arg213His
NM_001362850.1:c.638G>A NP_001349779.1:p.Arg213His
NM_000262.3:c.638G>A MANE Select NP_000253.1:p.Arg213His