Canonical Allele Identifier: CA2260527978

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538706A= , CM000679.2:g.42538706A=	GRCh38
NC_000017.10:g.40690724A= , CM000679.1:g.40690724A=	GRCh37
NC_000017.9:g.37944250A=	NCBI36
NG_011552.1:g.7774A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.715A= MANE Select	ENSP00000225927.1:p.Thr239=
ENST00000225927.6:c.715A=	ENSP00000225927.1:p.Thr239=
ENST00000586516.5:c.317A=
ENST00000591587.1:c.310A=	ENSP00000467836.1:p.Thr104=
NM_000263.3:c.715A=	NP_000254.2:p.Thr239=
XM_006721920.2:c.-28A=	XP_006721983.1:n.-28A=
XM_011524840.1:c.-28A=	XP_011523142.1:n.-28A=
XM_017024687.1:c.-28A=	XP_016880176.1:n.-28A=
XM_024450771.1:c.772A=	XP_024306539.1:p.Thr258=
XM_024450772.1:c.-28A=	XP_024306540.1:n.-28A=
NM_000263.4:c.715A= MANE Select	NP_000254.2:p.Thr239=