Canonical Allele Identifier: CA2260527827

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538391G= , CM000679.2:g.42538391G=	GRCh38
NC_000017.10:g.40690409G= , CM000679.1:g.40690409G=	GRCh37
NC_000017.9:g.37943935G=	NCBI36
NG_011552.1:g.7459G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.584G= MANE Select	ENSP00000225927.1:p.Gly195=
ENST00000225927.6:c.584G=	ENSP00000225927.1:p.Gly195=
ENST00000586516.5:c.186G=
ENST00000591587.1:c.179G=	ENSP00000467836.1:p.Gly60=
NM_000263.3:c.584G=	NP_000254.2:p.Gly195=
XM_006721920.2:c.-159G=	XP_006721983.1:n.-159G=
XM_011524840.1:c.-159G=	XP_011523142.1:n.-159G=
XM_017024687.1:c.-159G=	XP_016880176.1:n.-159G=
XM_024450771.1:c.641G=	XP_024306539.1:p.Gly214=
XM_024450772.1:c.-159G=	XP_024306540.1:n.-159G=
NM_000263.4:c.584G= MANE Select	NP_000254.2:p.Gly195=