Canonical Allele Identifier: CA2260526819

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42536563T= , CM000679.2:g.42536563T=	GRCh38
NC_000017.10:g.40688581T= , CM000679.1:g.40688581T=	GRCh37
NC_000017.9:g.37942107T=	NCBI36
NG_011552.1:g.5631T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.291T= MANE Select	ENSP00000225927.1:p.Cys97=
ENST00000225927.6:c.291T=	ENSP00000225927.1:p.Cys97=
ENST00000586516.5:c.41T=
ENST00000591587.1:c.34T=	ENSP00000467836.1:p.Trp12=
NM_000263.3:c.291T=	NP_000254.2:p.Cys97=
XM_006721920.2:c.-452T=	XP_006721983.1:n.-452T=
XM_011524840.1:c.-452T=	XP_011523142.1:n.-452T=
XM_024450771.1:c.291T=	XP_024306539.1:p.Cys97=
NM_000263.4:c.291T= MANE Select	NP_000254.2:p.Cys97=