Canonical Allele Identifier: CA2260526628
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536242T= , CM000679.2:g.42536242T= GRCh38
NC_000017.10:g.40688260T= , CM000679.1:g.40688260T= GRCh37
NC_000017.9:g.37941786T= NCBI36
NG_011552.1:g.5310T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.-31T= MANE Select ENSP00000225927.1:n.-31T=
ENST00000225927.6:c.-31T= ENSP00000225927.1:n.-31T=
NM_000263.3:c.-31T= NP_000254.2:n.-31T=
XM_024450771.1:c.-31T= XP_024306539.1:n.-31T=
NM_000263.4:c.-31T= MANE Select NP_000254.2:n.-31T=