Canonical Allele Identifier: CA500216631

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40693199T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42541181T>G , CM000679.2:g.42541181T>G	GRCh38
NC_000017.10:g.40693199T>G , CM000679.1:g.40693199T>G	GRCh37
NC_000017.9:g.37946725T>G	NCBI36
NG_011552.1:g.10249T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.996T>G MANE Select	ENSP00000225927.1:p.Thr332=
ENST00000225927.6:c.996T>G	ENSP00000225927.1:p.Thr332=
ENST00000591587.1:c.360-1847T>G	ENSP00000467836.1:n.360-1847T>G
ENST00000592454.1:c.91T>G
NM_000263.3:c.996T>G	NP_000254.2:p.Thr332=
XM_006721920.2:c.165T>G	XP_006721983.1:p.Thr55=
XM_011524840.1:c.23-1847T>G	XP_011523142.1:n.23-1847T>G
XM_017024687.1:c.165T>G	XP_016880176.1:p.Thr55=
XM_024450771.1:c.1053T>G	XP_024306539.1:p.Thr351=
XM_024450772.1:c.23-1847T>G	XP_024306540.1:n.23-1847T>G
NM_000263.4:c.996T>G MANE Select	NP_000254.2:p.Thr332=