Canonical Allele Identifier: CA2260526749

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42536442C= , CM000679.2:g.42536442C=	GRCh38
NC_000017.10:g.40688460C= , CM000679.1:g.40688460C=	GRCh37
NC_000017.9:g.37941986C=	NCBI36
NG_011552.1:g.5510C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.170C= MANE Select	ENSP00000225927.1:p.Ala57=
ENST00000225927.6:c.170C=	ENSP00000225927.1:p.Ala57=
NM_000263.3:c.170C=	NP_000254.2:p.Ala57=
XM_024450771.1:c.170C=	XP_024306539.1:p.Ala57=
NM_000263.4:c.170C= MANE Select	NP_000254.2:p.Ala57=