Canonical Allele Identifier: CA399598429

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40690403T>A (hg19) ; chr17:g.42538385T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538385T>A , CM000679.2:g.42538385T>A	GRCh38
NC_000017.10:g.40690403T>A , CM000679.1:g.40690403T>A	GRCh37
NC_000017.9:g.37943929T>A	NCBI36
NG_011552.1:g.7453T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000225927.7:c.578T>A MANE Select	ENSP00000225927.1:p.Phe193Tyr
ENST00000225927.6:c.578T>A	ENSP00000225927.1:p.Phe193Tyr
ENST00000586516.5:c.180T>A
ENST00000591587.1:c.173T>A	ENSP00000467836.1:p.Phe58Tyr
NM_000263.3:c.578T>A	NP_000254.2:p.Phe193Tyr
XM_006721920.2:c.-165T>A	XP_006721983.1:n.-165T>A
XM_011524840.1:c.-165T>A	XP_011523142.1:n.-165T>A
XM_017024687.1:c.-165T>A	XP_016880176.1:n.-165T>A
XM_024450771.1:c.635T>A	XP_024306539.1:p.Phe212Tyr
XM_024450772.1:c.-165T>A	XP_024306540.1:n.-165T>A
NM_000263.4:c.578T>A MANE Select	NP_000254.2:p.Phe193Tyr