Canonical Allele Identifier: CA2260530278

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543450C= , CM000679.2:g.42543450C=	GRCh38
NC_000017.10:g.40695468C= , CM000679.1:g.40695468C=	GRCh37
NC_000017.9:g.37948994C=	NCBI36
NG_011552.1:g.12518C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000263.4:c.1444C= MANE Select	NP_000254.2:p.Arg482=
ENST00000225927.7:c.1444C= MANE Select	ENSP00000225927.1:p.Arg482=
NM_000263.3:c.1444C=	NP_000254.2:p.Arg482=
ENST00000225927.6:c.1444C=	ENSP00000225927.1:p.Arg482=
ENST00000591587.1:c.782C=	ENSP00000467836.1:n.782C=
ENST00000592454.1:c.483C=
XM_006721920.2:c.613C=	XP_006721983.1:p.Arg205=
XM_011524840.1:c.445C=	XP_011523142.1:p.Arg149=
XM_017024687.1:c.613C=	XP_016880176.1:p.Arg205=
XM_024450771.1:c.1501C=	XP_024306539.1:p.Arg501=
XM_024450772.1:c.445C=	XP_024306540.1:p.Arg149=