Canonical Allele Identifier: CA399602403

Gene: NAGLU

Linked Data

• gnomAD v4: 17-42543421-C-A
• MyVariant Identifiers: chr17:g.40695439C>A (hg19) ; chr17:g.42543421C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543421C>A , CM000679.2:g.42543421C>A	GRCh38
NC_000017.10:g.40695439C>A , CM000679.1:g.40695439C>A	GRCh37
NC_000017.9:g.37948965C>A	NCBI36
NG_011552.1:g.12489C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.1415C>A MANE Select	ENSP00000225927.1:p.Ala472Glu
ENST00000225927.6:c.1415C>A	ENSP00000225927.1:p.Ala472Glu
ENST00000591587.1:c.753C>A	ENSP00000467836.1:n.753C>A
ENST00000592454.1:c.454C>A
NM_000263.3:c.1415C>A	NP_000254.2:p.Ala472Glu
XM_006721920.2:c.584C>A	XP_006721983.1:p.Ala195Glu
XM_011524840.1:c.416C>A	XP_011523142.1:p.Ala139Glu
XM_017024687.1:c.584C>A	XP_016880176.1:p.Ala195Glu
XM_024450771.1:c.1472C>A	XP_024306539.1:p.Ala491Glu
XM_024450772.1:c.416C>A	XP_024306540.1:p.Ala139Glu
NM_000263.4:c.1415C>A MANE Select	NP_000254.2:p.Ala472Glu