Canonical Allele Identifier: CA2577736655

Gene: NAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42060903_42060915del , CM000684.2:g.42060903_42060915del	GRCh38
NC_000022.10:g.42456907_42456919del , CM000684.1:g.42456907_42456919del	GRCh37
NC_000022.9:g.40786853_40786865del	NCBI36
NG_009247.1:g.14928_14940del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.1101+9_1101+21del MANE Select	ENSP00000379680.3:n.1101+9_1101+21del
ENST00000396398.7:c.1101+9_1101+21del	ENSP00000379680.3:n.1101+9_1101+21del
ENST00000402937.1:c.1101+9_1101+21del	ENSP00000384603.1:n.1101+9_1101+21del
ENST00000403363.5:c.1101+9_1101+21del	ENSP00000385283.1:n.1101+9_1101+21del
NM_000262.2:c.1101+9_1101+21del	NP_000253.1:n.1101+9_1101+21del
XM_005261615.3:c.1101+9_1101+21del	XP_005261672.1:n.1101+9_1101+21del
XM_005261616.3:c.1101+9_1101+21del	XP_005261673.1:n.1101+9_1101+21del
NM_001362848.1:c.1101+9_1101+21del	NP_001349777.1:n.1101+9_1101+21del
NM_001362850.1:c.1101+9_1101+21del	NP_001349779.1:n.1101+9_1101+21del
NM_000262.3:c.1101+9_1101+21del MANE Select	NP_000253.1:n.1101+9_1101+21del