Canonical Allele Identifier: CA2260526787

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42536503G= , CM000679.2:g.42536503G=	GRCh38
NC_000017.10:g.40688521G= , CM000679.1:g.40688521G=	GRCh37
NC_000017.9:g.37942047G=	NCBI36
NG_011552.1:g.5571G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.231G= MANE Select	ENSP00000225927.1:p.Val77=
ENST00000225927.6:c.231G=	ENSP00000225927.1:p.Val77=
NM_000263.3:c.231G=	NP_000254.2:p.Val77=
XM_024450771.1:c.231G=	XP_024306539.1:p.Val77=
NM_000263.4:c.231G= MANE Select	NP_000254.2:p.Val77=