Canonical Allele Identifier: CA399595961

Gene: NAGLU

Linked Data

• gnomAD v4: 17-42536558-T-A
• MyVariant Identifiers: chr17:g.40688576T>A (hg19) ; chr17:g.42536558T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42536558T>A , CM000679.2:g.42536558T>A	GRCh38
NC_000017.10:g.40688576T>A , CM000679.1:g.40688576T>A	GRCh37
NC_000017.9:g.37942102T>A	NCBI36
NG_011552.1:g.5626T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.286T>A MANE Select	ENSP00000225927.1:p.Phe96Ile
ENST00000225927.6:c.286T>A	ENSP00000225927.1:p.Phe96Ile
ENST00000586516.5:c.36T>A
ENST00000591587.1:c.29T>A	ENSP00000467836.1:p.Leu10His
NM_000263.3:c.286T>A	NP_000254.2:p.Phe96Ile
XM_006721920.2:c.-457T>A	XP_006721983.1:n.-457T>A
XM_011524840.1:c.-457T>A	XP_011523142.1:n.-457T>A
XM_024450771.1:c.286T>A	XP_024306539.1:p.Phe96Ile
NM_000263.4:c.286T>A MANE Select	NP_000254.2:p.Phe96Ile