Canonical Allele Identifier: CA2260529156

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42541100A= , CM000679.2:g.42541100A=	GRCh38
NC_000017.10:g.40693118A= , CM000679.1:g.40693118A=	GRCh37
NC_000017.9:g.37946644A=	NCBI36
NG_011552.1:g.10168A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.915A= MANE Select	ENSP00000225927.1:p.Thr305=
ENST00000225927.6:c.915A=	ENSP00000225927.1:p.Thr305=
ENST00000591587.1:c.360-1928A=	ENSP00000467836.1:n.360-1928A=
ENST00000592454.1:c.10A=
NM_000263.3:c.915A=	NP_000254.2:p.Thr305=
XM_006721920.2:c.84A=	XP_006721983.1:p.Thr28=
XM_011524840.1:c.23-1928A=	XP_011523142.1:n.23-1928A=
XM_017024687.1:c.84A=	XP_016880176.1:p.Thr28=
XM_024450771.1:c.972A=	XP_024306539.1:p.Thr324=
XM_024450772.1:c.23-1928A=	XP_024306540.1:n.23-1928A=
NM_000263.4:c.915A= MANE Select	NP_000254.2:p.Thr305=