Canonical Allele Identifier: CA500216581

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40693049T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42541031T>A , CM000679.2:g.42541031T>A	GRCh38
NC_000017.10:g.40693049T>A , CM000679.1:g.40693049T>A	GRCh37
NC_000017.9:g.37946575T>A	NCBI36
NG_011552.1:g.10099T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.846T>A MANE Select	ENSP00000225927.1:p.Ala282=
ENST00000225927.6:c.846T>A	ENSP00000225927.1:p.Ala282=
ENST00000586516.5:c.448T>A
ENST00000591587.1:c.360-1997T>A	ENSP00000467836.1:n.360-1997T>A
NM_000263.3:c.846T>A	NP_000254.2:p.Ala282=
XM_006721920.2:c.23-8T>A	XP_006721983.1:n.23-8T>A
XM_011524840.1:c.23-1997T>A	XP_011523142.1:n.23-1997T>A
XM_017024687.1:c.23-8T>A	XP_016880176.1:n.23-8T>A
XM_024450771.1:c.903T>A	XP_024306539.1:p.Ala301=
XM_024450772.1:c.23-1997T>A	XP_024306540.1:n.23-1997T>A
NM_000263.4:c.846T>A MANE Select	NP_000254.2:p.Ala282=