Canonical Allele Identifier: CA2577736649

Gene: NAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42060853_42060854insTA , CM000684.2:g.42060853_42060854insTA	GRCh38
NC_000022.10:g.42456857_42456858insTA , CM000684.1:g.42456857_42456858insTA	GRCh37
NC_000022.9:g.40786803_40786804insTA	NCBI36
NG_009247.1:g.14989_14990insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.1101+70_1101+71insTA MANE Select	ENSP00000379680.3:n.1101+70_1101+71insTA
ENST00000396398.7:c.1101+70_1101+71insTA	ENSP00000379680.3:n.1101+70_1101+71insTA
ENST00000402937.1:c.1101+70_1101+71insTA	ENSP00000384603.1:n.1101+70_1101+71insTA
ENST00000403363.5:c.1101+70_1101+71insTA	ENSP00000385283.1:n.1101+70_1101+71insTA
NM_000262.2:c.1101+70_1101+71insTA	NP_000253.1:n.1101+70_1101+71insTA
XM_005261615.3:c.1101+70_1101+71insTA	XP_005261672.1:n.1101+70_1101+71insTA
XM_005261616.3:c.1101+70_1101+71insTA	XP_005261673.1:n.1101+70_1101+71insTA
NM_001362848.1:c.1101+70_1101+71insTA	NP_001349777.1:n.1101+70_1101+71insTA
NM_001362850.1:c.1101+70_1101+71insTA	NP_001349779.1:n.1101+70_1101+71insTA
NM_000262.3:c.1101+70_1101+71insTA MANE Select	NP_000253.1:n.1101+70_1101+71insTA