Canonical Allele Identifier: CA399606214

Gene: NAGLU

Linked Data

• ClinVar Variation Id: 1471710
• ClinVar RCV Id: RCV002002717
• dbSNP Id: rs139195906
• MyVariant Identifiers: chr17:g.40696148C>G (hg19) ; chr17:g.42544130C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544130C>G , CM000679.2:g.42544130C>G	GRCh38
NC_000017.10:g.40696148C>G , CM000679.1:g.40696148C>G	GRCh37
NC_000017.9:g.37949674C>G	NCBI36
NG_011552.1:g.13198C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2124C>G MANE Select	ENSP00000225927.1:p.Phe708Leu
ENST00000225927.6:c.2124C>G	ENSP00000225927.1:p.Phe708Leu
ENST00000591587.1:c.1462C>G	ENSP00000467836.1:n.1462C>G
NM_000263.3:c.2124C>G	NP_000254.2:p.Phe708Leu
XM_006721920.2:c.1293C>G	XP_006721983.1:p.Phe431Leu
XM_011524840.1:c.1125C>G	XP_011523142.1:p.Phe375Leu
XM_017024687.1:c.1293C>G	XP_016880176.1:p.Phe431Leu
XM_024450771.1:c.2181C>G	XP_024306539.1:p.Phe727Leu
XM_024450772.1:c.1125C>G	XP_024306540.1:p.Phe375Leu
NM_000263.4:c.2124C>G MANE Select	NP_000254.2:p.Phe708Leu