Canonical Allele Identifier: CA10263882

Gene: NAGA

Linked Data

• dbSNP Id: rs778804889
• ExAC: 22:42463801 A / C
• gnomAD v2: 22-42463801-A-C
• gnomAD v4: 22-42067797-A-C
• MyVariant Identifiers: chr22:g.42463801A>C (hg19) ; chr22:g.42067797A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42067797A>C , CM000684.2:g.42067797A>C	GRCh38
NC_000022.10:g.42463801A>C , CM000684.1:g.42463801A>C	GRCh37
NC_000022.9:g.40793747A>C	NCBI36
NG_009247.1:g.8046T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.292T>G MANE Select	ENSP00000379680.3:p.Phe98Val
ENST00000396398.7:c.292T>G	ENSP00000379680.3:p.Phe98Val
ENST00000402937.1:c.292T>G	ENSP00000384603.1:p.Phe98Val
ENST00000403363.5:c.292T>G	ENSP00000385283.1:p.Phe98Val
NM_000262.2:c.292T>G	NP_000253.1:p.Phe98Val
XM_005261615.3:c.292T>G	XP_005261672.1:p.Phe98Val
XM_005261616.3:c.292T>G	XP_005261673.1:p.Phe98Val
NM_001362848.1:c.292T>G	NP_001349777.1:p.Phe98Val
NM_001362850.1:c.292T>G	NP_001349779.1:p.Phe98Val
NM_000262.3:c.292T>G MANE Select	NP_000253.1:p.Phe98Val