Canonical Allele Identifier: CA2260526805
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536534G= , CM000679.2:g.42536534G= GRCh38
NC_000017.10:g.40688552G= , CM000679.1:g.40688552G= GRCh37
NC_000017.9:g.37942078G= NCBI36
NG_011552.1:g.5602G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.262G= MANE Select ENSP00000225927.1:p.Gly88=
ENST00000225927.6:c.262G= ENSP00000225927.1:p.Gly88=
ENST00000586516.5:c.12G=
ENST00000591587.1:c.5G= ENSP00000467836.1:p.Gly2=
NM_000263.3:c.262G= NP_000254.2:p.Gly88=
XM_024450771.1:c.262G= XP_024306539.1:p.Gly88=
NM_000263.4:c.262G= MANE Select NP_000254.2:p.Gly88=