Canonical Allele Identifier: CA8577077
Gene: NAGLU HGNC NCBI

Linked Data

dbSNP Id: rs766911974

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42543686G>A , CM000679.2:g.42543686G>A GRCh38
NC_000017.10:g.40695704G>A , CM000679.1:g.40695704G>A GRCh37
NC_000017.9:g.37949230G>A NCBI36
NG_011552.1:g.12754G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.1680G>A MANE Select ENSP00000225927.1:p.Leu560=
ENST00000225927.6:c.1680G>A ENSP00000225927.1:p.Leu560=
ENST00000591587.1:c.1018G>A ENSP00000467836.1:n.1018G>A
NM_000263.3:c.1680G>A NP_000254.2:p.Leu560=
XM_006721920.2:c.849G>A XP_006721983.1:p.Leu283=
XM_011524840.1:c.681G>A XP_011523142.1:p.Leu227=
XM_017024687.1:c.849G>A XP_016880176.1:p.Leu283=
XM_024450771.1:c.1737G>A XP_024306539.1:p.Leu579=
XM_024450772.1:c.681G>A XP_024306540.1:p.Leu227=
NM_000263.4:c.1680G>A MANE Select NP_000254.2:p.Leu560=