Canonical Allele Identifier: CA2260526967
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536809C= , CM000679.2:g.42536809C= GRCh38
NC_000017.10:g.40688827C= , CM000679.1:g.40688827C= GRCh37
NC_000017.9:g.37942353C= NCBI36
NG_011552.1:g.5877C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.383+154C= MANE Select ENSP00000225927.1:n.383+154C=
ENST00000225927.6:c.383+154C= ENSP00000225927.1:n.383+154C=
ENST00000586516.5:c.133+154C=
ENST00000591587.1:c.126+154C= ENSP00000467836.1:n.126+154C=
NM_000263.3:c.383+154C= NP_000254.2:n.383+154C=
XM_006721920.2:c.-360+154C= XP_006721983.1:n.-360+154C=
XM_011524840.1:c.-360+154C= XP_011523142.1:n.-360+154C=
XM_024450771.1:c.384-8C= XP_024306539.1:n.384-8C=
NM_000263.4:c.383+154C= MANE Select NP_000254.2:n.383+154C=