Canonical Allele Identifier: CA399604043

Gene: NAGLU

Linked Data

• dbSNP Id: rs2092927759
• gnomAD v3: 17-42543511-A-G
• gnomAD v4: 17-42543511-A-G
• MyVariant Identifiers: chr17:g.40695529A>G (hg19) ; chr17:g.42543511A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543511A>G , CM000679.2:g.42543511A>G	GRCh38
NC_000017.10:g.40695529A>G , CM000679.1:g.40695529A>G	GRCh37
NC_000017.9:g.37949055A>G	NCBI36
NG_011552.1:g.12579A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1505A>G MANE Select	ENSP00000225927.1:p.Tyr502Cys
ENST00000225927.6:c.1505A>G	ENSP00000225927.1:p.Tyr502Cys
ENST00000591587.1:c.843A>G	ENSP00000467836.1:n.843A>G
ENST00000592454.1:c.544A>G
NM_000263.3:c.1505A>G	NP_000254.2:p.Tyr502Cys
XM_006721920.2:c.674A>G	XP_006721983.1:p.Tyr225Cys
XM_011524840.1:c.506A>G	XP_011523142.1:p.Tyr169Cys
XM_017024687.1:c.674A>G	XP_016880176.1:p.Tyr225Cys
XM_024450771.1:c.1562A>G	XP_024306539.1:p.Tyr521Cys
XM_024450772.1:c.506A>G	XP_024306540.1:p.Tyr169Cys
NM_000263.4:c.1505A>G MANE Select	NP_000254.2:p.Tyr502Cys