Canonical Allele Identifier: CA2406550539

Gene: NAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42067064G= , CM000684.2:g.42067064G=	GRCh38
NC_000022.10:g.42463068G= , CM000684.1:g.42463068G=	GRCh37
NC_000022.9:g.40793014G=	NCBI36
NG_009247.1:g.8779C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396398.8:c.502+49C= MANE Select	ENSP00000379680.3:n.502+49C=
ENST00000396398.7:c.502+49C=	ENSP00000379680.3:n.502+49C=
ENST00000402937.1:c.502+49C=	ENSP00000384603.1:n.502+49C=
ENST00000403363.5:c.502+49C=	ENSP00000385283.1:n.502+49C=
NM_000262.2:c.502+49C=	NP_000253.1:n.502+49C=
XM_005261615.3:c.502+49C=	XP_005261672.1:n.502+49C=
XM_005261616.3:c.502+49C=	XP_005261673.1:n.502+49C=
NM_001362848.1:c.502+49C=	NP_001349777.1:n.502+49C=
NM_001362850.1:c.502+49C=	NP_001349779.1:n.502+49C=
NM_000262.3:c.502+49C= MANE Select	NP_000253.1:n.502+49C=