Canonical Allele Identifier: CA399606139

Gene: NAGLU

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2093A>C MANE Select	ENSP00000225927.1:p.Asp698Ala
ENST00000225927.6:c.2093A>C	ENSP00000225927.1:p.Asp698Ala
ENST00000591587.1:c.1431A>C	ENSP00000467836.1:n.1431A>C
NM_000263.3:c.2093A>C	NP_000254.2:p.Asp698Ala
XM_006721920.2:c.1262A>C	XP_006721983.1:p.Asp421Ala
XM_011524840.1:c.1094A>C	XP_011523142.1:p.Asp365Ala
XM_017024687.1:c.1262A>C	XP_016880176.1:p.Asp421Ala
XM_024450771.1:c.2150A>C	XP_024306539.1:p.Asp717Ala
XM_024450772.1:c.1094A>C	XP_024306540.1:p.Asp365Ala
NM_000263.4:c.2093A>C MANE Select	NP_000254.2:p.Asp698Ala