Canonical Allele Identifier: CA2406550451

Gene: NAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42066835_42066836delinsAG , CM000684.2:g.42066835_42066836delinsAG	GRCh38
NC_000022.10:g.42462839_42462840delinsAG , CM000684.1:g.42462839_42462840delinsAG	GRCh37
NC_000022.9:g.40792785_40792786delinsAG	NCBI36
NG_009247.1:g.9007_9008delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.503-32_503-31delinsCT MANE Select	ENSP00000379680.3:n.503-32_503-31delinsCT
ENST00000396398.7:c.503-32_503-31delinsCT	ENSP00000379680.3:n.503-32_503-31delinsCT
ENST00000402937.1:c.503-32_503-31delinsCT	ENSP00000384603.1:n.503-32_503-31delinsCT
ENST00000403363.5:c.503-32_503-31delinsCT	ENSP00000385283.1:n.503-32_503-31delinsCT
NM_000262.2:c.503-32_503-31delinsCT	NP_000253.1:n.503-32_503-31delinsCT
XM_005261615.3:c.503-32_503-31delinsCT	XP_005261672.1:n.503-32_503-31delinsCT
XM_005261616.3:c.503-32_503-31delinsCT	XP_005261673.1:n.503-32_503-31delinsCT
NM_001362848.1:c.503-32_503-31delinsCT	NP_001349777.1:n.503-32_503-31delinsCT
NM_001362850.1:c.503-32_503-31delinsCT	NP_001349779.1:n.503-32_503-31delinsCT
NM_000262.3:c.503-32_503-31delinsCT MANE Select	NP_000253.1:n.503-32_503-31delinsCT