Canonical Allele Identifier: CA399605099

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40695870T>A (hg19) ; chr17:g.42543852T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42543852T>A , CM000679.2:g.42543852T>A	GRCh38
NC_000017.10:g.40695870T>A , CM000679.1:g.40695870T>A	GRCh37
NC_000017.9:g.37949396T>A	NCBI36
NG_011552.1:g.12920T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.1846T>A MANE Select	ENSP00000225927.1:p.Phe616Ile
ENST00000225927.6:c.1846T>A	ENSP00000225927.1:p.Phe616Ile
ENST00000591587.1:c.1184T>A	ENSP00000467836.1:n.1184T>A
NM_000263.3:c.1846T>A	NP_000254.2:p.Phe616Ile
XM_006721920.2:c.1015T>A	XP_006721983.1:p.Phe339Ile
XM_011524840.1:c.847T>A	XP_011523142.1:p.Phe283Ile
XM_017024687.1:c.1015T>A	XP_016880176.1:p.Phe339Ile
XM_024450771.1:c.1903T>A	XP_024306539.1:p.Phe635Ile
XM_024450772.1:c.847T>A	XP_024306540.1:p.Phe283Ile
NM_000263.4:c.1846T>A MANE Select	NP_000254.2:p.Phe616Ile