Canonical Allele Identifier: CA10263600

Gene: NAGA

Linked Data

• dbSNP Id: rs750968203
• ExAC: 22:42456912 GCA / G
• gnomAD v2: 22-42456912-GCA-G
• gnomAD v3: 22-42060908-GCA-G
• gnomAD v4: 22-42060908-GCA-G
• MyVariant Identifiers: chr22:g.42456913_42456914del (hg19) ; chr22:g.42060909_42060910del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42060909_42060910del , CM000684.2:g.42060909_42060910del	GRCh38
NC_000022.10:g.42456913_42456914del , CM000684.1:g.42456913_42456914del	GRCh37
NC_000022.9:g.40786859_40786860del	NCBI36
NG_009247.1:g.14933_14934del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.1101+14_1101+15del MANE Select	ENSP00000379680.3:n.1101+14_1101+15del
ENST00000396398.7:c.1101+14_1101+15del	ENSP00000379680.3:n.1101+14_1101+15del
ENST00000402937.1:c.1101+14_1101+15del	ENSP00000384603.1:n.1101+14_1101+15del
ENST00000403363.5:c.1101+14_1101+15del	ENSP00000385283.1:n.1101+14_1101+15del
NM_000262.2:c.1101+14_1101+15del	NP_000253.1:n.1101+14_1101+15del
XM_005261615.3:c.1101+14_1101+15del	XP_005261672.1:n.1101+14_1101+15del
XM_005261616.3:c.1101+14_1101+15del	XP_005261673.1:n.1101+14_1101+15del
NM_001362848.1:c.1101+14_1101+15del	NP_001349777.1:n.1101+14_1101+15del
NM_001362850.1:c.1101+14_1101+15del	NP_001349779.1:n.1101+14_1101+15del
NM_000262.3:c.1101+14_1101+15del MANE Select	NP_000253.1:n.1101+14_1101+15del