Canonical Allele Identifier: CA2260526736
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536416C= , CM000679.2:g.42536416C= GRCh38
NC_000017.10:g.40688434C= , CM000679.1:g.40688434C= GRCh37
NC_000017.9:g.37941960C= NCBI36
NG_011552.1:g.5484C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.144C= MANE Select ENSP00000225927.1:p.Phe48=
ENST00000225927.6:c.144C= ENSP00000225927.1:p.Phe48=
NM_000263.3:c.144C= NP_000254.2:p.Phe48=
XM_024450771.1:c.144C= XP_024306539.1:p.Phe48=
NM_000263.4:c.144C= MANE Select NP_000254.2:p.Phe48=