Canonical Allele Identifier: CA500217626

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40696163G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544145G>A , CM000679.2:g.42544145G>A	GRCh38
NC_000017.10:g.40696163G>A , CM000679.1:g.40696163G>A	GRCh37
NC_000017.9:g.37949689G>A	NCBI36
NG_011552.1:g.13213G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2139G>A MANE Select	ENSP00000225927.1:p.Gln713=
ENST00000225927.6:c.2139G>A	ENSP00000225927.1:p.Gln713=
ENST00000591587.1:c.1477G>A	ENSP00000467836.1:n.1477G>A
NM_000263.3:c.2139G>A	NP_000254.2:p.Gln713=
XM_006721920.2:c.1308G>A	XP_006721983.1:p.Gln436=
XM_011524840.1:c.1140G>A	XP_011523142.1:p.Gln380=
XM_017024687.1:c.1308G>A	XP_016880176.1:p.Gln436=
XM_024450771.1:c.2196G>A	XP_024306539.1:p.Gln732=
XM_024450772.1:c.1140G>A	XP_024306540.1:p.Gln380=
NM_000263.4:c.2139G>A MANE Select	NP_000254.2:p.Gln713=