Canonical Allele Identifier: CA2260526689
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536316T= , CM000679.2:g.42536316T= GRCh38
NC_000017.10:g.40688334T= , CM000679.1:g.40688334T= GRCh37
NC_000017.9:g.37941860T= NCBI36
NG_011552.1:g.5384T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.44T= MANE Select ENSP00000225927.1:p.Leu15=
ENST00000225927.6:c.44T= ENSP00000225927.1:p.Leu15=
NM_000263.3:c.44T= NP_000254.2:p.Leu15=
XM_024450771.1:c.44T= XP_024306539.1:p.Leu15=
NM_000263.4:c.44T= MANE Select NP_000254.2:p.Leu15=