Canonical Allele Identifier: CA399604432

Gene: NAGLU

Linked Data

• ClinVar Variation Id: 2927301
• ClinVar RCV Id: RCV003781491
• gnomAD v4: 17-42543681-G-T
• MyVariant Identifiers: chr17:g.40695699G>T (hg19) ; chr17:g.42543681G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543681G>T , CM000679.2:g.42543681G>T	GRCh38
NC_000017.10:g.40695699G>T , CM000679.1:g.40695699G>T	GRCh37
NC_000017.9:g.37949225G>T	NCBI36
NG_011552.1:g.12749G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1675G>T MANE Select	ENSP00000225927.1:p.Asp559Tyr
ENST00000225927.6:c.1675G>T	ENSP00000225927.1:p.Asp559Tyr
ENST00000591587.1:c.1013G>T	ENSP00000467836.1:n.1013G>T
NM_000263.3:c.1675G>T	NP_000254.2:p.Asp559Tyr
XM_006721920.2:c.844G>T	XP_006721983.1:p.Asp282Tyr
XM_011524840.1:c.676G>T	XP_011523142.1:p.Asp226Tyr
XM_017024687.1:c.844G>T	XP_016880176.1:p.Asp282Tyr
XM_024450771.1:c.1732G>T	XP_024306539.1:p.Asp578Tyr
XM_024450772.1:c.676G>T	XP_024306540.1:p.Asp226Tyr
NM_000263.4:c.1675G>T MANE Select	NP_000254.2:p.Asp559Tyr