Canonical Allele Identifier: CA2406547849

Gene: NAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42061262_42061265delinsCTCA , CM000684.2:g.42061262_42061265delinsCTCA	GRCh38
NC_000022.10:g.42457266_42457269delinsCTCA , CM000684.1:g.42457266_42457269delinsCTCA	GRCh37
NC_000022.9:g.40787212_40787215delinsCTCA	NCBI36
NG_009247.1:g.14578_14581delinsTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.958-198_958-195delinsTGAG MANE Select	ENSP00000379680.3:n.958-198_958-195delinsTGAG
ENST00000396398.7:c.958-198_958-195delinsTGAG	ENSP00000379680.3:n.958-198_958-195delinsTGAG
ENST00000402937.1:c.958-198_958-195delinsTGAG	ENSP00000384603.1:n.958-198_958-195delinsTGAG
ENST00000403363.5:c.958-198_958-195delinsTGAG	ENSP00000385283.1:n.958-198_958-195delinsTGAG
NM_000262.2:c.958-198_958-195delinsTGAG	NP_000253.1:n.958-198_958-195delinsTGAG
XM_005261615.3:c.958-198_958-195delinsTGAG	XP_005261672.1:n.958-198_958-195delinsTGAG
XM_005261616.3:c.958-198_958-195delinsTGAG	XP_005261673.1:n.958-198_958-195delinsTGAG
NM_001362848.1:c.958-198_958-195delinsTGAG	NP_001349777.1:n.958-198_958-195delinsTGAG
NM_001362850.1:c.958-198_958-195delinsTGAG	NP_001349779.1:n.958-198_958-195delinsTGAG
NM_000262.3:c.958-198_958-195delinsTGAG MANE Select	NP_000253.1:n.958-198_958-195delinsTGAG