Canonical Allele Identifier: CA399606486

Gene: NAGLU

Linked Data

• MyVariant Identifiers: chr17:g.40696237G>C (hg19) ; chr17:g.42544219G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42544219G>C , CM000679.2:g.42544219G>C	GRCh38
NC_000017.10:g.40696237G>C , CM000679.1:g.40696237G>C	GRCh37
NC_000017.9:g.37949763G>C	NCBI36
NG_011552.1:g.13287G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225927.7:c.2213G>C MANE Select	ENSP00000225927.1:p.Trp738Ser
ENST00000225927.6:c.2213G>C	ENSP00000225927.1:p.Trp738Ser
NM_000263.3:c.2213G>C	NP_000254.2:p.Trp738Ser
XM_006721920.2:c.1382G>C	XP_006721983.1:p.Trp461Ser
XM_011524840.1:c.1214G>C	XP_011523142.1:p.Trp405Ser
XM_017024687.1:c.1382G>C	XP_016880176.1:p.Trp461Ser
XM_024450771.1:c.2270G>C	XP_024306539.1:p.Trp757Ser
XM_024450772.1:c.1214G>C	XP_024306540.1:p.Trp405Ser
NM_000263.4:c.2213G>C MANE Select	NP_000254.2:p.Trp738Ser