Canonical Allele Identifier: CA2260530320

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543514A= , CM000679.2:g.42543514A=	GRCh38
NC_000017.10:g.40695532A= , CM000679.1:g.40695532A=	GRCh37
NC_000017.9:g.37949058A=	NCBI36
NG_011552.1:g.12582A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1508A= MANE Select	ENSP00000225927.1:p.Asn503=
ENST00000225927.6:c.1508A=	ENSP00000225927.1:p.Asn503=
ENST00000591587.1:c.846A=	ENSP00000467836.1:n.846A=
ENST00000592454.1:c.547A=
NM_000263.3:c.1508A=	NP_000254.2:p.Asn503=
XM_006721920.2:c.677A=	XP_006721983.1:p.Asn226=
XM_011524840.1:c.509A=	XP_011523142.1:p.Asn170=
XM_017024687.1:c.677A=	XP_016880176.1:p.Asn226=
XM_024450771.1:c.1565A=	XP_024306539.1:p.Asn522=
XM_024450772.1:c.509A=	XP_024306540.1:p.Asn170=
NM_000263.4:c.1508A= MANE Select	NP_000254.2:p.Asn503=