Canonical Allele Identifier: CA411768519

Gene: NAGA

Linked Data

• gnomAD v4: 22-42066754-A-T
• MyVariant Identifiers: chr22:g.42462758A>T (hg19) ; chr22:g.42066754A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42066754A>T , CM000684.2:g.42066754A>T	GRCh38
NC_000022.10:g.42462758A>T , CM000684.1:g.42462758A>T	GRCh37
NC_000022.9:g.40792704A>T	NCBI36
NG_009247.1:g.9089T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.553T>A MANE Select	ENSP00000379680.3:p.Phe185Ile
ENST00000396398.7:c.553T>A	ENSP00000379680.3:p.Phe185Ile
ENST00000402937.1:c.553T>A	ENSP00000384603.1:p.Phe185Ile
ENST00000403363.5:c.553T>A	ENSP00000385283.1:p.Phe185Ile
NM_000262.2:c.553T>A	NP_000253.1:p.Phe185Ile
XM_005261615.3:c.553T>A	XP_005261672.1:p.Phe185Ile
XM_005261616.3:c.553T>A	XP_005261673.1:p.Phe185Ile
NM_001362848.1:c.553T>A	NP_001349777.1:p.Phe185Ile
NM_001362850.1:c.553T>A	NP_001349779.1:p.Phe185Ile
NM_000262.3:c.553T>A MANE Select	NP_000253.1:p.Phe185Ile