Canonical Allele Identifier: CA10263595

Gene: NAGA

Linked Data

• dbSNP Id: rs781686372
• ExAC: 22:42456892 GC / G
• gnomAD v2: 22-42456892-GC-G
• gnomAD v3: 22-42060888-GC-G
• gnomAD v4: 22-42060888-GC-G
• MyVariant Identifiers: chr22:g.42456893del (hg19) ; chr22:g.42060889del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42060891del , CM000684.2:g.42060891del	GRCh38
NC_000022.10:g.42456895del , CM000684.1:g.42456895del	GRCh37
NC_000022.9:g.40786841del	NCBI36
NG_009247.1:g.14954del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.1101+35del MANE Select	ENSP00000379680.3:n.1101+35del
ENST00000396398.7:c.1101+35del	ENSP00000379680.3:n.1101+35del
ENST00000402937.1:c.1101+35del	ENSP00000384603.1:n.1101+35del
ENST00000403363.5:c.1101+35del	ENSP00000385283.1:n.1101+35del
NM_000262.2:c.1101+35del	NP_000253.1:n.1101+35del
XM_005261615.3:c.1101+35del	XP_005261672.1:n.1101+35del
XM_005261616.3:c.1101+35del	XP_005261673.1:n.1101+35del
NM_001362848.1:c.1101+35del	NP_001349777.1:n.1101+35del
NM_001362850.1:c.1101+35del	NP_001349779.1:n.1101+35del
NM_000262.3:c.1101+35del MANE Select	NP_000253.1:n.1101+35del