Canonical Allele Identifier: CA399606141

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40696117A>T (hg19) ; chr17:g.42544099A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544099A>T , CM000679.2:g.42544099A>T	GRCh38
NC_000017.10:g.40696117A>T , CM000679.1:g.40696117A>T	GRCh37
NC_000017.9:g.37949643A>T	NCBI36
NG_011552.1:g.13167A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2093A>T MANE Select	ENSP00000225927.1:p.Asp698Val
ENST00000225927.6:c.2093A>T	ENSP00000225927.1:p.Asp698Val
ENST00000591587.1:c.1431A>T	ENSP00000467836.1:n.1431A>T
NM_000263.3:c.2093A>T	NP_000254.2:p.Asp698Val
XM_006721920.2:c.1262A>T	XP_006721983.1:p.Asp421Val
XM_011524840.1:c.1094A>T	XP_011523142.1:p.Asp365Val
XM_017024687.1:c.1262A>T	XP_016880176.1:p.Asp421Val
XM_024450771.1:c.2150A>T	XP_024306539.1:p.Asp717Val
XM_024450772.1:c.1094A>T	XP_024306540.1:p.Asp365Val
NM_000263.4:c.2093A>T MANE Select	NP_000254.2:p.Asp698Val