Canonical Allele Identifier: CA2260528022

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538778C= , CM000679.2:g.42538778C=	GRCh38
NC_000017.10:g.40690796C= , CM000679.1:g.40690796C=	GRCh37
NC_000017.9:g.37944322C=	NCBI36
NG_011552.1:g.7846C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.764+23C= MANE Select	ENSP00000225927.1:n.764+23C=
ENST00000225927.6:c.764+23C=	ENSP00000225927.1:n.764+23C=
ENST00000586516.5:c.366+23C=
ENST00000591587.1:c.359+23C=	ENSP00000467836.1:n.359+23C=
NM_000263.3:c.764+23C=	NP_000254.2:n.764+23C=
XM_006721920.2:c.22+23C=	XP_006721983.1:n.22+23C=
XM_011524840.1:c.22+23C=	XP_011523142.1:n.22+23C=
XM_017024687.1:c.22+23C=	XP_016880176.1:n.22+23C=
XM_024450771.1:c.821+23C=	XP_024306539.1:n.821+23C=
XM_024450772.1:c.22+23C=	XP_024306540.1:n.22+23C=
NM_000263.4:c.764+23C= MANE Select	NP_000254.2:n.764+23C=