Canonical Allele Identifier: CA2260530472

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543817C= , CM000679.2:g.42543817C=	GRCh38
NC_000017.10:g.40695835C= , CM000679.1:g.40695835C=	GRCh37
NC_000017.9:g.37949361C=	NCBI36
NG_011552.1:g.12885C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1811C= MANE Select	ENSP00000225927.1:p.Pro604=
ENST00000225927.6:c.1811C=	ENSP00000225927.1:p.Pro604=
ENST00000591587.1:c.1149C=	ENSP00000467836.1:n.1149C=
NM_000263.3:c.1811C=	NP_000254.2:p.Pro604=
XM_006721920.2:c.980C=	XP_006721983.1:p.Pro327=
XM_011524840.1:c.812C=	XP_011523142.1:p.Pro271=
XM_017024687.1:c.980C=	XP_016880176.1:p.Pro327=
XM_024450771.1:c.1868C=	XP_024306539.1:p.Pro623=
XM_024450772.1:c.812C=	XP_024306540.1:p.Pro271=
NM_000263.4:c.1811C= MANE Select	NP_000254.2:p.Pro604=