Canonical Allele Identifier: CA2260526721
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536384C= , CM000679.2:g.42536384C= GRCh38
NC_000017.10:g.40688402C= , CM000679.1:g.40688402C= GRCh37
NC_000017.9:g.37941928C= NCBI36
NG_011552.1:g.5452C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.112C= MANE Select ENSP00000225927.1:p.Arg38=
ENST00000225927.6:c.112C= ENSP00000225927.1:p.Arg38=
NM_000263.3:c.112C= NP_000254.2:p.Arg38=
XM_024450771.1:c.112C= XP_024306539.1:p.Arg38=
NM_000263.4:c.112C= MANE Select NP_000254.2:p.Arg38=