Canonical Allele Identifier: CA2260529270

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42541301T= , CM000679.2:g.42541301T=	GRCh38
NC_000017.10:g.40693319T= , CM000679.1:g.40693319T=	GRCh37
NC_000017.9:g.37946845T=	NCBI36
NG_011552.1:g.10369T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1021+95T= MANE Select	ENSP00000225927.1:n.1021+95T=
ENST00000225927.6:c.1021+95T=	ENSP00000225927.1:n.1021+95T=
ENST00000591587.1:c.360-1727T=	ENSP00000467836.1:n.360-1727T=
ENST00000592454.1:c.116+95T=
NM_000263.3:c.1021+95T=	NP_000254.2:n.1021+95T=
XM_006721920.2:c.190+95T=	XP_006721983.1:n.190+95T=
XM_011524840.1:c.23-1727T=	XP_011523142.1:n.23-1727T=
XM_017024687.1:c.190+95T=	XP_016880176.1:n.190+95T=
XM_024450771.1:c.1078+95T=	XP_024306539.1:n.1078+95T=
XM_024450772.1:c.23-1727T=	XP_024306540.1:n.23-1727T=
NM_000263.4:c.1021+95T= MANE Select	NP_000254.2:n.1021+95T=