Canonical Allele Identifier: CA2260526745
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536431G= , CM000679.2:g.42536431G= GRCh38
NC_000017.10:g.40688449G= , CM000679.1:g.40688449G= GRCh37
NC_000017.9:g.37941975G= NCBI36
NG_011552.1:g.5499G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.159G= MANE Select ENSP00000225927.1:p.Glu53=
ENST00000225927.6:c.159G= ENSP00000225927.1:p.Glu53=
NM_000263.3:c.159G= NP_000254.2:p.Glu53=
XM_024450771.1:c.159G= XP_024306539.1:p.Glu53=
NM_000263.4:c.159G= MANE Select NP_000254.2:p.Glu53=