Canonical Allele Identifier: CA2260526697
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536327G= , CM000679.2:g.42536327G= GRCh38
NC_000017.10:g.40688345G= , CM000679.1:g.40688345G= GRCh37
NC_000017.9:g.37941871G= NCBI36
NG_011552.1:g.5395G=

Transcript Alleles

HGVS Amino-acid change
ENST00000225927.7:c.55G= MANE Select ENSP00000225927.1:p.Gly19=
ENST00000225927.6:c.55G= ENSP00000225927.1:p.Gly19=
NM_000263.3:c.55G= NP_000254.2:p.Gly19=
XM_024450771.1:c.55G= XP_024306539.1:p.Gly19=
NM_000263.4:c.55G= MANE Select NP_000254.2:p.Gly19=