Canonical Allele Identifier: CA399598422

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40690400T>C (hg19) ; chr17:g.42538382T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42538382T>C , CM000679.2:g.42538382T>C	GRCh38
NC_000017.10:g.40690400T>C , CM000679.1:g.40690400T>C	GRCh37
NC_000017.9:g.37943926T>C	NCBI36
NG_011552.1:g.7450T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.575T>C MANE Select	ENSP00000225927.1:p.Phe192Ser
ENST00000225927.6:c.575T>C	ENSP00000225927.1:p.Phe192Ser
ENST00000586516.5:c.177T>C
ENST00000591587.1:c.170T>C	ENSP00000467836.1:p.Phe57Ser
NM_000263.3:c.575T>C	NP_000254.2:p.Phe192Ser
XM_006721920.2:c.-168T>C	XP_006721983.1:n.-168T>C
XM_011524840.1:c.-168T>C	XP_011523142.1:n.-168T>C
XM_017024687.1:c.-168T>C	XP_016880176.1:n.-168T>C
XM_024450771.1:c.632T>C	XP_024306539.1:p.Phe211Ser
XM_024450772.1:c.-168T>C	XP_024306540.1:n.-168T>C
NM_000263.4:c.575T>C MANE Select	NP_000254.2:p.Phe192Ser