Canonical Allele Identifier: CA399604232

Gene: NAGLU

Linked Data

• gnomAD v4: 17-42543594-T-G
• MyVariant Identifiers: chr17:g.40695612T>G (hg19) ; chr17:g.42543594T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543594T>G , CM000679.2:g.42543594T>G	GRCh38
NC_000017.10:g.40695612T>G , CM000679.1:g.40695612T>G	GRCh37
NC_000017.9:g.37949138T>G	NCBI36
NG_011552.1:g.12662T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1588T>G MANE Select	ENSP00000225927.1:p.Trp530Gly
ENST00000225927.6:c.1588T>G	ENSP00000225927.1:p.Trp530Gly
ENST00000591587.1:c.926T>G	ENSP00000467836.1:n.926T>G
NM_000263.3:c.1588T>G	NP_000254.2:p.Trp530Gly
XM_006721920.2:c.757T>G	XP_006721983.1:p.Trp253Gly
XM_011524840.1:c.589T>G	XP_011523142.1:p.Trp197Gly
XM_017024687.1:c.757T>G	XP_016880176.1:p.Trp253Gly
XM_024450771.1:c.1645T>G	XP_024306539.1:p.Trp549Gly
XM_024450772.1:c.589T>G	XP_024306540.1:p.Trp197Gly
NM_000263.4:c.1588T>G MANE Select	NP_000254.2:p.Trp530Gly