Canonical Allele Identifier: CA10651428

Gene: NAGA

Linked Data

• ClinVar Variation Id: 341901
• ClinVar RCV Id: RCV000270304 ; RCV000327782
• dbSNP Id: rs761125179
• gnomAD v2: 22-42456128-T-C
• gnomAD v3: 22-42060124-T-C
• gnomAD v4: 22-42060124-T-C
• MyVariant Identifiers: chr22:g.42456128T>C (hg19) ; chr22:g.42060124T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42060124T>C , CM000684.2:g.42060124T>C	GRCh38
NC_000022.10:g.42456128T>C , CM000684.1:g.42456128T>C	GRCh37
NC_000022.9:g.40786074T>C	NCBI36
NG_009247.1:g.15719A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.*155A>G MANE Select	ENSP00000379680.3:n.*155A>G
ENST00000396398.7:c.*155A>G	ENSP00000379680.3:n.*155A>G
ENST00000402937.1:c.*155A>G	ENSP00000384603.1:n.*155A>G
ENST00000403363.5:c.*155A>G	ENSP00000385283.1:n.*155A>G
NM_000262.2:c.*155A>G	NP_000253.1:n.*155A>G
XM_005261615.3:c.*155A>G	XP_005261672.1:n.*155A>G
XM_005261616.3:c.*155A>G	XP_005261673.1:n.*155A>G
NM_001362848.1:c.*155A>G	NP_001349777.1:n.*155A>G
NM_001362850.1:c.*155A>G	NP_001349779.1:n.*155A>G
NM_000262.3:c.*155A>G MANE Select	NP_000253.1:n.*155A>G