Canonical Allele Identifier: CA2260526661
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536276G= , CM000679.2:g.42536276G= GRCh38
NC_000017.10:g.40688294G= , CM000679.1:g.40688294G= GRCh37
NC_000017.9:g.37941820G= NCBI36
NG_011552.1:g.5344G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.4G= MANE Select ENSP00000225927.1:p.Glu2=
ENST00000225927.6:c.4G= ENSP00000225927.1:p.Glu2=
NM_000263.3:c.4G= NP_000254.2:p.Glu2=
XM_024450771.1:c.4G= XP_024306539.1:p.Glu2=
NM_000263.4:c.4G= MANE Select NP_000254.2:p.Glu2=