Canonical Allele Identifier: CA2260529298

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42541360C= , CM000679.2:g.42541360C=	GRCh38
NC_000017.10:g.40693378C= , CM000679.1:g.40693378C=	GRCh37
NC_000017.9:g.37946904C=	NCBI36
NG_011552.1:g.10428C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1021+154C= MANE Select	ENSP00000225927.1:n.1021+154C=
ENST00000225927.6:c.1021+154C=	ENSP00000225927.1:n.1021+154C=
ENST00000591587.1:c.360-1668C=	ENSP00000467836.1:n.360-1668C=
ENST00000592454.1:c.116+154C=
NM_000263.3:c.1021+154C=	NP_000254.2:n.1021+154C=
XM_006721920.2:c.190+154C=	XP_006721983.1:n.190+154C=
XM_011524840.1:c.23-1668C=	XP_011523142.1:n.23-1668C=
XM_017024687.1:c.190+154C=	XP_016880176.1:n.190+154C=
XM_024450771.1:c.1078+154C=	XP_024306539.1:n.1078+154C=
XM_024450772.1:c.23-1668C=	XP_024306540.1:n.23-1668C=
NM_000263.4:c.1021+154C= MANE Select	NP_000254.2:n.1021+154C=