Canonical Allele Identifier: CA2406550269

Gene: NAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42066467_42066468delinsCA , CM000684.2:g.42066467_42066468delinsCA	GRCh38
NC_000022.10:g.42462471_42462472delinsCA , CM000684.1:g.42462471_42462472delinsCA	GRCh37
NC_000022.9:g.40792417_40792418delinsCA	NCBI36
NG_009247.1:g.9375_9376delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.597+242_597+243delinsTG MANE Select	ENSP00000379680.3:n.597+242_597+243delinsTG
ENST00000396398.7:c.597+242_597+243delinsTG	ENSP00000379680.3:n.597+242_597+243delinsTG
ENST00000402937.1:c.597+242_597+243delinsTG	ENSP00000384603.1:n.597+242_597+243delinsTG
ENST00000403363.5:c.597+242_597+243delinsTG	ENSP00000385283.1:n.597+242_597+243delinsTG
NM_000262.2:c.597+242_597+243delinsTG	NP_000253.1:n.597+242_597+243delinsTG
XM_005261615.3:c.597+242_597+243delinsTG	XP_005261672.1:n.597+242_597+243delinsTG
XM_005261616.3:c.597+242_597+243delinsTG	XP_005261673.1:n.597+242_597+243delinsTG
NM_001362848.1:c.597+242_597+243delinsTG	NP_001349777.1:n.597+242_597+243delinsTG
NM_001362850.1:c.597+242_597+243delinsTG	NP_001349779.1:n.597+242_597+243delinsTG
NM_000262.3:c.597+242_597+243delinsTG MANE Select	NP_000253.1:n.597+242_597+243delinsTG