Canonical Allele Identifier: CA2260526821

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42536569C= , CM000679.2:g.42536569C=	GRCh38
NC_000017.10:g.40688587C= , CM000679.1:g.40688587C=	GRCh37
NC_000017.9:g.37942113C=	NCBI36
NG_011552.1:g.5637C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.297C= MANE Select	ENSP00000225927.1:p.Cys99=
ENST00000225927.6:c.297C=	ENSP00000225927.1:p.Cys99=
ENST00000586516.5:c.47C=
ENST00000591587.1:c.40C=	ENSP00000467836.1:p.Pro14=
NM_000263.3:c.297C=	NP_000254.2:p.Cys99=
XM_006721920.2:c.-446C=	XP_006721983.1:n.-446C=
XM_011524840.1:c.-446C=	XP_011523142.1:n.-446C=
XM_024450771.1:c.297C=	XP_024306539.1:p.Cys99=
NM_000263.4:c.297C= MANE Select	NP_000254.2:p.Cys99=