Canonical Allele Identifier: CA2260530548

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543965C= , CM000679.2:g.42543965C=	GRCh38
NC_000017.10:g.40695983C= , CM000679.1:g.40695983C=	GRCh37
NC_000017.9:g.37949509C=	NCBI36
NG_011552.1:g.13033C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.1959C= MANE Select	ENSP00000225927.1:p.Gly653=
ENST00000225927.6:c.1959C=	ENSP00000225927.1:p.Gly653=
ENST00000591587.1:c.1297C=	ENSP00000467836.1:n.1297C=
NM_000263.3:c.1959C=	NP_000254.2:p.Gly653=
XM_006721920.2:c.1128C=	XP_006721983.1:p.Gly376=
XM_011524840.1:c.960C=	XP_011523142.1:p.Gly320=
XM_017024687.1:c.1128C=	XP_016880176.1:p.Gly376=
XM_024450771.1:c.2016C=	XP_024306539.1:p.Gly672=
XM_024450772.1:c.960C=	XP_024306540.1:p.Gly320=
NM_000263.4:c.1959C= MANE Select	NP_000254.2:p.Gly653=