Canonical Allele Identifier: CA290781065

Gene: NAGLU

Linked Data

• dbSNP Id: rs112510624
• gnomAD v2: 17-40695868-G-A
• gnomAD v3: 17-42543850-G-A
• gnomAD v4: 17-42543850-G-A
• MyVariant Identifiers: chr17:g.40695868G>A (hg19) ; chr17:g.42543850G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543850G>A , CM000679.2:g.42543850G>A	GRCh38
NC_000017.10:g.40695868G>A , CM000679.1:g.40695868G>A	GRCh37
NC_000017.9:g.37949394G>A	NCBI36
NG_011552.1:g.12918G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.1844G>A MANE Select	ENSP00000225927.1:p.Arg615His
ENST00000225927.6:c.1844G>A	ENSP00000225927.1:p.Arg615His
ENST00000591587.1:c.1182G>A	ENSP00000467836.1:n.1182G>A
NM_000263.3:c.1844G>A	NP_000254.2:p.Arg615His
XM_006721920.2:c.1013G>A	XP_006721983.1:p.Arg338His
XM_011524840.1:c.845G>A	XP_011523142.1:p.Arg282His
XM_017024687.1:c.1013G>A	XP_016880176.1:p.Arg338His
XM_024450771.1:c.1901G>A	XP_024306539.1:p.Arg634His
XM_024450772.1:c.845G>A	XP_024306540.1:p.Arg282His
NM_000263.4:c.1844G>A MANE Select	NP_000254.2:p.Arg615His