Canonical Allele Identifier: CA2260530466

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543803C= , CM000679.2:g.42543803C=	GRCh38
NC_000017.10:g.40695821C= , CM000679.1:g.40695821C=	GRCh37
NC_000017.9:g.37949347C=	NCBI36
NG_011552.1:g.12871C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1797C= MANE Select	ENSP00000225927.1:p.Ala599=
ENST00000225927.6:c.1797C=	ENSP00000225927.1:p.Ala599=
ENST00000591587.1:c.1135C=	ENSP00000467836.1:n.1135C=
NM_000263.3:c.1797C=	NP_000254.2:p.Ala599=
XM_006721920.2:c.966C=	XP_006721983.1:p.Ala322=
XM_011524840.1:c.798C=	XP_011523142.1:p.Ala266=
XM_017024687.1:c.966C=	XP_016880176.1:p.Ala322=
XM_024450771.1:c.1854C=	XP_024306539.1:p.Ala618=
XM_024450772.1:c.798C=	XP_024306540.1:p.Ala266=
NM_000263.4:c.1797C= MANE Select	NP_000254.2:p.Ala599=