Canonical Allele Identifier: CA399606509

Gene: NAGLU

Linked Data

• ClinVar Variation Id: 1911534
• ClinVar RCV Id: RCV002597024
• gnomAD v4: 17-42544224-G-A
• MyVariant Identifiers: chr17:g.40696242G>A (hg19) ; chr17:g.42544224G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544224G>A , CM000679.2:g.42544224G>A	GRCh38
NC_000017.10:g.40696242G>A , CM000679.1:g.40696242G>A	GRCh37
NC_000017.9:g.37949768G>A	NCBI36
NG_011552.1:g.13292G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2218G>A MANE Select	ENSP00000225927.1:p.Ala740Thr
ENST00000225927.6:c.2218G>A	ENSP00000225927.1:p.Ala740Thr
NM_000263.3:c.2218G>A	NP_000254.2:p.Ala740Thr
XM_006721920.2:c.1387G>A	XP_006721983.1:p.Ala463Thr
XM_011524840.1:c.1219G>A	XP_011523142.1:p.Ala407Thr
XM_017024687.1:c.1387G>A	XP_016880176.1:p.Ala463Thr
XM_024450771.1:c.2275G>A	XP_024306539.1:p.Ala759Thr
XM_024450772.1:c.1219G>A	XP_024306540.1:p.Ala407Thr
NM_000263.4:c.2218G>A MANE Select	NP_000254.2:p.Ala740Thr