Canonical Allele Identifier: CA2260530357

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543579A= , CM000679.2:g.42543579A=	GRCh38
NC_000017.10:g.40695597A= , CM000679.1:g.40695597A=	GRCh37
NC_000017.9:g.37949123A=	NCBI36
NG_011552.1:g.12647A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1573A= MANE Select	ENSP00000225927.1:p.Met525=
ENST00000225927.6:c.1573A=	ENSP00000225927.1:p.Met525=
ENST00000591587.1:c.911A=	ENSP00000467836.1:n.911A=
NM_000263.3:c.1573A=	NP_000254.2:p.Met525=
XM_006721920.2:c.742A=	XP_006721983.1:p.Met248=
XM_011524840.1:c.574A=	XP_011523142.1:p.Met192=
XM_017024687.1:c.742A=	XP_016880176.1:p.Met248=
XM_024450771.1:c.1630A=	XP_024306539.1:p.Met544=
XM_024450772.1:c.574A=	XP_024306540.1:p.Met192=
NM_000263.4:c.1573A= MANE Select	NP_000254.2:p.Met525=