Canonical Allele Identifier: CA2260530229

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543356G= , CM000679.2:g.42543356G=	GRCh38
NC_000017.10:g.40695374G= , CM000679.1:g.40695374G=	GRCh37
NC_000017.9:g.37948900G=	NCBI36
NG_011552.1:g.12424G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1350G= MANE Select	ENSP00000225927.1:p.Gln450=
ENST00000225927.6:c.1350G=	ENSP00000225927.1:p.Gln450=
ENST00000591587.1:c.688G=	ENSP00000467836.1:n.688G=
ENST00000592454.1:c.389G=
NM_000263.3:c.1350G=	NP_000254.2:p.Gln450=
XM_006721920.2:c.519G=	XP_006721983.1:p.Gln173=
XM_011524840.1:c.351G=	XP_011523142.1:p.Gln117=
XM_017024687.1:c.519G=	XP_016880176.1:p.Gln173=
XM_024450771.1:c.1407G=	XP_024306539.1:p.Gln469=
XM_024450772.1:c.351G=	XP_024306540.1:p.Gln117=
NM_000263.4:c.1350G= MANE Select	NP_000254.2:p.Gln450=