Canonical Allele Identifier: CA2406550232

Gene: NAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42066366_42066367delinsTG , CM000684.2:g.42066366_42066367delinsTG	GRCh38
NC_000022.10:g.42462370_42462371delinsTG , CM000684.1:g.42462370_42462371delinsTG	GRCh37
NC_000022.9:g.40792316_40792317delinsTG	NCBI36
NG_009247.1:g.9476_9477delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.597+343_597+344delinsCA MANE Select	ENSP00000379680.3:n.597+343_597+344delinsCA
ENST00000396398.7:c.597+343_597+344delinsCA	ENSP00000379680.3:n.597+343_597+344delinsCA
ENST00000402937.1:c.597+343_597+344delinsCA	ENSP00000384603.1:n.597+343_597+344delinsCA
ENST00000403363.5:c.597+343_597+344delinsCA	ENSP00000385283.1:n.597+343_597+344delinsCA
NM_000262.2:c.597+343_597+344delinsCA	NP_000253.1:n.597+343_597+344delinsCA
XM_005261615.3:c.597+343_597+344delinsCA	XP_005261672.1:n.597+343_597+344delinsCA
XM_005261616.3:c.597+343_597+344delinsCA	XP_005261673.1:n.597+343_597+344delinsCA
NM_001362848.1:c.597+343_597+344delinsCA	NP_001349777.1:n.597+343_597+344delinsCA
NM_001362850.1:c.597+343_597+344delinsCA	NP_001349779.1:n.597+343_597+344delinsCA
NM_000262.3:c.597+343_597+344delinsCA MANE Select	NP_000253.1:n.597+343_597+344delinsCA