Canonical Allele Identifier: CA2260530658

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544211C= , CM000679.2:g.42544211C=	GRCh38
NC_000017.10:g.40696229C= , CM000679.1:g.40696229C=	GRCh37
NC_000017.9:g.37949755C=	NCBI36
NG_011552.1:g.13279C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2205C= MANE Select	ENSP00000225927.1:p.Tyr735=
ENST00000225927.6:c.2205C=	ENSP00000225927.1:p.Tyr735=
NM_000263.3:c.2205C=	NP_000254.2:p.Tyr735=
XM_006721920.2:c.1374C=	XP_006721983.1:p.Tyr458=
XM_011524840.1:c.1206C=	XP_011523142.1:p.Tyr402=
XM_017024687.1:c.1374C=	XP_016880176.1:p.Tyr458=
XM_024450771.1:c.2262C=	XP_024306539.1:p.Tyr754=
XM_024450772.1:c.1206C=	XP_024306540.1:p.Tyr402=
NM_000263.4:c.2205C= MANE Select	NP_000254.2:p.Tyr735=