Canonical Allele Identifier: CA2260530493

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543878G= , CM000679.2:g.42543878G=	GRCh38
NC_000017.10:g.40695896G= , CM000679.1:g.40695896G=	GRCh37
NC_000017.9:g.37949422G=	NCBI36
NG_011552.1:g.12946G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1872G= MANE Select	ENSP00000225927.1:p.Gln624=
ENST00000225927.6:c.1872G=	ENSP00000225927.1:p.Gln624=
ENST00000591587.1:c.1210G=	ENSP00000467836.1:n.1210G=
NM_000263.3:c.1872G=	NP_000254.2:p.Gln624=
XM_006721920.2:c.1041G=	XP_006721983.1:p.Gln347=
XM_011524840.1:c.873G=	XP_011523142.1:p.Gln291=
XM_017024687.1:c.1041G=	XP_016880176.1:p.Gln347=
XM_024450771.1:c.1929G=	XP_024306539.1:p.Gln643=
XM_024450772.1:c.873G=	XP_024306540.1:p.Gln291=
NM_000263.4:c.1872G= MANE Select	NP_000254.2:p.Gln624=