Canonical Allele Identifier: CA2260526932

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42536744G= , CM000679.2:g.42536744G=	GRCh38
NC_000017.10:g.40688762G= , CM000679.1:g.40688762G=	GRCh37
NC_000017.9:g.37942288G=	NCBI36
NG_011552.1:g.5812G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.383+89G= MANE Select	ENSP00000225927.1:n.383+89G=
ENST00000225927.6:c.383+89G=	ENSP00000225927.1:n.383+89G=
ENST00000586516.5:c.133+89G=
ENST00000591587.1:c.126+89G=	ENSP00000467836.1:n.126+89G=
NM_000263.3:c.383+89G=	NP_000254.2:n.383+89G=
XM_006721920.2:c.-360+89G=	XP_006721983.1:n.-360+89G=
XM_011524840.1:c.-360+89G=	XP_011523142.1:n.-360+89G=
XM_024450771.1:c.384-73G=	XP_024306539.1:n.384-73G=
NM_000263.4:c.383+89G= MANE Select	NP_000254.2:n.383+89G=