Canonical Allele Identifier: CA399604844

Gene: NAGLU

Linked Data

• ClinVar Variation Id: 1491845
• ClinVar RCV Id: RCV001988942
• dbSNP Id: rs1274337932
• gnomAD v2: 17-40695802-G-A
• gnomAD v4: 17-42543784-G-A
• MyVariant Identifiers: chr17:g.40695802G>A (hg19) ; chr17:g.42543784G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543784G>A , CM000679.2:g.42543784G>A	GRCh38
NC_000017.10:g.40695802G>A , CM000679.1:g.40695802G>A	GRCh37
NC_000017.9:g.37949328G>A	NCBI36
NG_011552.1:g.12852G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1778G>A MANE Select	ENSP00000225927.1:p.Arg593Lys
ENST00000225927.6:c.1778G>A	ENSP00000225927.1:p.Arg593Lys
ENST00000591587.1:c.1116G>A	ENSP00000467836.1:n.1116G>A
NM_000263.3:c.1778G>A	NP_000254.2:p.Arg593Lys
XM_006721920.2:c.947G>A	XP_006721983.1:p.Arg316Lys
XM_011524840.1:c.779G>A	XP_011523142.1:p.Arg260Lys
XM_017024687.1:c.947G>A	XP_016880176.1:p.Arg316Lys
XM_024450771.1:c.1835G>A	XP_024306539.1:p.Arg612Lys
XM_024450772.1:c.779G>A	XP_024306540.1:p.Arg260Lys
NM_000263.4:c.1778G>A MANE Select	NP_000254.2:p.Arg593Lys