Canonical Allele Identifier: CA2260530672

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544227G= , CM000679.2:g.42544227G=	GRCh38
NC_000017.10:g.40696245G= , CM000679.1:g.40696245G=	GRCh37
NC_000017.9:g.37949771G=	NCBI36
NG_011552.1:g.13295G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2221G= MANE Select	ENSP00000225927.1:p.Gly741=
ENST00000225927.6:c.2221G=	ENSP00000225927.1:p.Gly741=
NM_000263.3:c.2221G=	NP_000254.2:p.Gly741=
XM_006721920.2:c.1390G=	XP_006721983.1:p.Gly464=
XM_011524840.1:c.1222G=	XP_011523142.1:p.Gly408=
XM_017024687.1:c.1390G=	XP_016880176.1:p.Gly464=
XM_024450771.1:c.2278G=	XP_024306539.1:p.Gly760=
XM_024450772.1:c.1222G=	XP_024306540.1:p.Gly408=
NM_000263.4:c.2221G= MANE Select	NP_000254.2:p.Gly741=