Canonical Allele Identifier: CA399601652

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40695289C>A (hg19) ; chr17:g.42543271C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543271C>A , CM000679.2:g.42543271C>A	GRCh38
NC_000017.10:g.40695289C>A , CM000679.1:g.40695289C>A	GRCh37
NC_000017.9:g.37948815C>A	NCBI36
NG_011552.1:g.12339C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.1265C>A MANE Select	ENSP00000225927.1:p.Ala422Asp
ENST00000225927.6:c.1265C>A	ENSP00000225927.1:p.Ala422Asp
ENST00000591587.1:c.603C>A	ENSP00000467836.1:n.603C>A
ENST00000592454.1:c.304C>A
NM_000263.3:c.1265C>A	NP_000254.2:p.Ala422Asp
XM_006721920.2:c.434C>A	XP_006721983.1:p.Ala145Asp
XM_011524840.1:c.266C>A	XP_011523142.1:p.Ala89Asp
XM_017024687.1:c.434C>A	XP_016880176.1:p.Ala145Asp
XM_024450771.1:c.1322C>A	XP_024306539.1:p.Ala441Asp
XM_024450772.1:c.266C>A	XP_024306540.1:p.Ala89Asp
NM_000263.4:c.1265C>A MANE Select	NP_000254.2:p.Ala422Asp