Canonical Allele Identifier: CA2406547680

Gene: NAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42060888_42060890delinsGCC , CM000684.2:g.42060888_42060890delinsGCC	GRCh38
NC_000022.10:g.42456892_42456894delinsGCC , CM000684.1:g.42456892_42456894delinsGCC	GRCh37
NC_000022.9:g.40786838_40786840delinsGCC	NCBI36
NG_009247.1:g.14953_14955delinsGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.1101+34_1101+36delinsGGC MANE Select	ENSP00000379680.3:n.1101+34_1101+36delinsGGC
ENST00000396398.7:c.1101+34_1101+36delinsGGC	ENSP00000379680.3:n.1101+34_1101+36delinsGGC
ENST00000402937.1:c.1101+34_1101+36delinsGGC	ENSP00000384603.1:n.1101+34_1101+36delinsGGC
ENST00000403363.5:c.1101+34_1101+36delinsGGC	ENSP00000385283.1:n.1101+34_1101+36delinsGGC
NM_000262.2:c.1101+34_1101+36delinsGGC	NP_000253.1:n.1101+34_1101+36delinsGGC
XM_005261615.3:c.1101+34_1101+36delinsGGC	XP_005261672.1:n.1101+34_1101+36delinsGGC
XM_005261616.3:c.1101+34_1101+36delinsGGC	XP_005261673.1:n.1101+34_1101+36delinsGGC
NM_001362848.1:c.1101+34_1101+36delinsGGC	NP_001349777.1:n.1101+34_1101+36delinsGGC
NM_001362850.1:c.1101+34_1101+36delinsGGC	NP_001349779.1:n.1101+34_1101+36delinsGGC
NM_000262.3:c.1101+34_1101+36delinsGGC MANE Select	NP_000253.1:n.1101+34_1101+36delinsGGC