Canonical Allele Identifier: CA2637971661
Gene: NAGLU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42543853del , CM000679.2:g.42543853del GRCh38
NC_000017.10:g.40695871del , CM000679.1:g.40695871del GRCh37
NC_000017.9:g.37949397del NCBI36
NG_011552.1:g.12921del

Transcript Alleles

HGVS Amino-acid change
ENST00000225927.7:c.1847del MANE Select ENSP00000225927.1:p.Phe616SerfsTer7
ENST00000225927.6:c.1847del ENSP00000225927.1:p.Phe616SerfsTer7
ENST00000591587.1:c.1185del ENSP00000467836.1:n.1185del
NM_000263.3:c.1847del NP_000254.2:p.Phe616SerfsTer7
XM_006721920.2:c.1016del XP_006721983.1:p.Phe339SerfsTer7
XM_011524840.1:c.848del XP_011523142.1:p.Phe283SerfsTer7
XM_017024687.1:c.1016del XP_016880176.1:p.Phe339SerfsTer7
XM_024450771.1:c.1904del XP_024306539.1:p.Phe635SerfsTer7
XM_024450772.1:c.848del XP_024306540.1:p.Phe283SerfsTer7
NM_000263.4:c.1847del MANE Select NP_000254.2:p.Phe616SerfsTer7