Canonical Allele Identifier: CA2260526635
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536247G= , CM000679.2:g.42536247G= GRCh38
NC_000017.10:g.40688265G= , CM000679.1:g.40688265G= GRCh37
NC_000017.9:g.37941791G= NCBI36
NG_011552.1:g.5315G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.-26G= MANE Select ENSP00000225927.1:n.-26G=
ENST00000225927.6:c.-26G= ENSP00000225927.1:n.-26G=
NM_000263.3:c.-26G= NP_000254.2:n.-26G=
XM_024450771.1:c.-26G= XP_024306539.1:n.-26G=
NM_000263.4:c.-26G= MANE Select NP_000254.2:n.-26G=