Canonical Allele Identifier: CA2260530194

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543284C= , CM000679.2:g.42543284C=	GRCh38
NC_000017.10:g.40695302C= , CM000679.1:g.40695302C=	GRCh37
NC_000017.9:g.37948828C=	NCBI36
NG_011552.1:g.12352C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1278C= MANE Select	ENSP00000225927.1:p.Gly426=
ENST00000225927.6:c.1278C=	ENSP00000225927.1:p.Gly426=
ENST00000591587.1:c.616C=	ENSP00000467836.1:n.616C=
ENST00000592454.1:c.317C=
NM_000263.3:c.1278C=	NP_000254.2:p.Gly426=
XM_006721920.2:c.447C=	XP_006721983.1:p.Gly149=
XM_011524840.1:c.279C=	XP_011523142.1:p.Gly93=
XM_017024687.1:c.447C=	XP_016880176.1:p.Gly149=
XM_024450771.1:c.1335C=	XP_024306539.1:p.Gly445=
XM_024450772.1:c.279C=	XP_024306540.1:p.Gly93=
NM_000263.4:c.1278C= MANE Select	NP_000254.2:p.Gly426=