Canonical Allele Identifier: CA2533140661
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42544266del , CM000679.2:g.42544266del GRCh38
NC_000017.10:g.40696284del , CM000679.1:g.40696284del GRCh37
NC_000017.9:g.37949810del NCBI36
NG_011552.1:g.13334del

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.*28del MANE Select ENSP00000225927.1:n.*28del
ENST00000225927.6:c.*28del ENSP00000225927.1:n.*28del
NM_000263.3:c.*28del NP_000254.2:n.*28del
XM_006721920.2:c.*28del XP_006721983.1:n.*28del
XM_011524840.1:c.*28del XP_011523142.1:n.*28del
XM_017024687.1:c.*28del XP_016880176.1:n.*28del
XM_024450771.1:c.*28del XP_024306539.1:n.*28del
XM_024450772.1:c.*28del XP_024306540.1:n.*28del
NM_000263.4:c.*28del MANE Select NP_000254.2:n.*28del