Canonical Allele Identifier: CA2260526828

Gene: NAGLU

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42536580G= , CM000679.2:g.42536580G=	GRCh38
NC_000017.10:g.40688598G= , CM000679.1:g.40688598G=	GRCh37
NC_000017.9:g.37942124G=	NCBI36
NG_011552.1:g.5648G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.308G= MANE Select	ENSP00000225927.1:p.Trp103=
ENST00000225927.6:c.308G=	ENSP00000225927.1:p.Trp103=
ENST00000586516.5:c.58G=
ENST00000591587.1:c.51G=	ENSP00000467836.1:p.Leu17=
NM_000263.3:c.308G=	NP_000254.2:p.Trp103=
XM_006721920.2:c.-435G=	XP_006721983.1:n.-435G=
XM_011524840.1:c.-435G=	XP_011523142.1:n.-435G=
XM_024450771.1:c.308G=	XP_024306539.1:p.Trp103=
NM_000263.4:c.308G= MANE Select	NP_000254.2:p.Trp103=