Canonical Allele Identifier: CA2406550429
Gene: NAGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42066778T= , CM000684.2:g.42066778T= GRCh38
NC_000022.10:g.42462782T= , CM000684.1:g.42462782T= GRCh37
NC_000022.9:g.40792728T= NCBI36
NG_009247.1:g.9065A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396398.8:c.529A= MANE Select ENSP00000379680.3:p.Asn177=
ENST00000396398.7:c.529A= ENSP00000379680.3:p.Asn177=
ENST00000402937.1:c.529A= ENSP00000384603.1:p.Asn177=
ENST00000403363.5:c.529A= ENSP00000385283.1:p.Asn177=
NM_000262.2:c.529A= NP_000253.1:p.Asn177=
XM_005261615.3:c.529A= XP_005261672.1:p.Asn177=
XM_005261616.3:c.529A= XP_005261673.1:p.Asn177=
NM_001362848.1:c.529A= NP_001349777.1:p.Asn177=
NM_001362850.1:c.529A= NP_001349779.1:p.Asn177=
NM_000262.3:c.529A= MANE Select NP_000253.1:p.Asn177=