Canonical Allele Identifier: CA2260526643
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536254G= , CM000679.2:g.42536254G= GRCh38
NC_000017.10:g.40688272G= , CM000679.1:g.40688272G= GRCh37
NC_000017.9:g.37941798G= NCBI36
NG_011552.1:g.5322G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.-19G= MANE Select ENSP00000225927.1:n.-19G=
ENST00000225927.6:c.-19G= ENSP00000225927.1:n.-19G=
NM_000263.3:c.-19G= NP_000254.2:n.-19G=
XM_024450771.1:c.-19G= XP_024306539.1:n.-19G=
NM_000263.4:c.-19G= MANE Select NP_000254.2:n.-19G=