Canonical Allele Identifier: CA2260526636
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536249C= , CM000679.2:g.42536249C= GRCh38
NC_000017.10:g.40688267C= , CM000679.1:g.40688267C= GRCh37
NC_000017.9:g.37941793C= NCBI36
NG_011552.1:g.5317C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.-24C= MANE Select ENSP00000225927.1:n.-24C=
ENST00000225927.6:c.-24C= ENSP00000225927.1:n.-24C=
NM_000263.3:c.-24C= NP_000254.2:n.-24C=
XM_024450771.1:c.-24C= XP_024306539.1:n.-24C=
NM_000263.4:c.-24C= MANE Select NP_000254.2:n.-24C=