Canonical Allele Identifier: CA753287242

Gene: NAGA

Linked Data

• dbSNP Id: rs1426013739
• MyVariant Identifiers: chr22:g.42462529_42462533del (hg19) ; chr22:g.42066525_42066529del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42066527_42066531del , CM000684.2:g.42066527_42066531del	GRCh38
NC_000022.10:g.42462531_42462535del , CM000684.1:g.42462531_42462535del	GRCh37
NC_000022.9:g.40792477_40792481del	NCBI36
NG_009247.1:g.9314_9318del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.597+181_597+185del MANE Select	ENSP00000379680.3:n.597+181_597+185del
ENST00000396398.7:c.597+181_597+185del	ENSP00000379680.3:n.597+181_597+185del
ENST00000402937.1:c.597+181_597+185del	ENSP00000384603.1:n.597+181_597+185del
ENST00000403363.5:c.597+181_597+185del	ENSP00000385283.1:n.597+181_597+185del
NM_000262.2:c.597+181_597+185del	NP_000253.1:n.597+181_597+185del
XM_005261615.3:c.597+181_597+185del	XP_005261672.1:n.597+181_597+185del
XM_005261616.3:c.597+181_597+185del	XP_005261673.1:n.597+181_597+185del
NM_001362848.1:c.597+181_597+185del	NP_001349777.1:n.597+181_597+185del
NM_001362850.1:c.597+181_597+185del	NP_001349779.1:n.597+181_597+185del
NM_000262.3:c.597+181_597+185del MANE Select	NP_000253.1:n.597+181_597+185del