Canonical Allele Identifier: CA2260529131

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42541043C= , CM000679.2:g.42541043C=	GRCh38
NC_000017.10:g.40693061C= , CM000679.1:g.40693061C=	GRCh37
NC_000017.9:g.37946587C=	NCBI36
NG_011552.1:g.10111C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.858C= MANE Select	ENSP00000225927.1:p.Pro286=
ENST00000225927.6:c.858C=	ENSP00000225927.1:p.Pro286=
ENST00000586516.5:c.460C=
ENST00000591587.1:c.360-1985C=	ENSP00000467836.1:n.360-1985C=
NM_000263.3:c.858C=	NP_000254.2:p.Pro286=
XM_006721920.2:c.27C=	XP_006721983.1:p.Pro9=
XM_011524840.1:c.23-1985C=	XP_011523142.1:n.23-1985C=
XM_017024687.1:c.27C=	XP_016880176.1:p.Pro9=
XM_024450771.1:c.915C=	XP_024306539.1:p.Pro305=
XM_024450772.1:c.23-1985C=	XP_024306540.1:n.23-1985C=
NM_000263.4:c.858C= MANE Select	NP_000254.2:p.Pro286=