Canonical Allele Identifier: CA290780757

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543564C>T , CM000679.2:g.42543564C>T	GRCh38
NC_000017.10:g.40695582C>T , CM000679.1:g.40695582C>T	GRCh37
NC_000017.9:g.37949108C>T	NCBI36
NG_011552.1:g.12632C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000263.4:c.1558C>T MANE Select	NP_000254.2:p.Arg520Trp
ENST00000225927.7:c.1558C>T MANE Select	ENSP00000225927.1:p.Arg520Trp
NM_000263.3:c.1558C>T	NP_000254.2:p.Arg520Trp
ENST00000225927.6:c.1558C>T	ENSP00000225927.1:p.Arg520Trp
ENST00000591587.1:c.896C>T	ENSP00000467836.1:n.896C>T
XM_006721920.2:c.727C>T	XP_006721983.1:p.Arg243Trp
XM_011524840.1:c.559C>T	XP_011523142.1:p.Arg187Trp
XM_017024687.1:c.727C>T	XP_016880176.1:p.Arg243Trp
XM_024450771.1:c.1615C>T	XP_024306539.1:p.Arg539Trp
XM_024450772.1:c.559C>T	XP_024306540.1:p.Arg187Trp