Canonical Allele Identifier: CA2260530641

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544164C= , CM000679.2:g.42544164C=	GRCh38
NC_000017.10:g.40696182C= , CM000679.1:g.40696182C=	GRCh37
NC_000017.9:g.37949708C=	NCBI36
NG_011552.1:g.13232C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2158C= MANE Select	ENSP00000225927.1:p.Arg720=
ENST00000225927.6:c.2158C=	ENSP00000225927.1:p.Arg720=
NM_000263.3:c.2158C=	NP_000254.2:p.Arg720=
XM_006721920.2:c.1327C=	XP_006721983.1:p.Arg443=
XM_011524840.1:c.1159C=	XP_011523142.1:p.Arg387=
XM_017024687.1:c.1327C=	XP_016880176.1:p.Arg443=
XM_024450771.1:c.2215C=	XP_024306539.1:p.Arg739=
XM_024450772.1:c.1159C=	XP_024306540.1:p.Arg387=
NM_000263.4:c.2158C= MANE Select	NP_000254.2:p.Arg720=