Canonical Allele Identifier: CA2260530398

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543669G= , CM000679.2:g.42543669G=	GRCh38
NC_000017.10:g.40695687G= , CM000679.1:g.40695687G=	GRCh37
NC_000017.9:g.37949213G=	NCBI36
NG_011552.1:g.12737G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1663G= MANE Select	ENSP00000225927.1:p.Ala555=
ENST00000225927.6:c.1663G=	ENSP00000225927.1:p.Ala555=
ENST00000591587.1:c.1001G=	ENSP00000467836.1:n.1001G=
NM_000263.3:c.1663G=	NP_000254.2:p.Ala555=
XM_006721920.2:c.832G=	XP_006721983.1:p.Ala278=
XM_011524840.1:c.664G=	XP_011523142.1:p.Ala222=
XM_017024687.1:c.832G=	XP_016880176.1:p.Ala278=
XM_024450771.1:c.1720G=	XP_024306539.1:p.Ala574=
XM_024450772.1:c.664G=	XP_024306540.1:p.Ala222=
NM_000263.4:c.1663G= MANE Select	NP_000254.2:p.Ala555=