Canonical Allele Identifier: CA2260527934
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42538599T= , CM000679.2:g.42538599T= GRCh38
NC_000017.10:g.40690617T= , CM000679.1:g.40690617T= GRCh37
NC_000017.9:g.37944143T= NCBI36
NG_011552.1:g.7667T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.679-71T= MANE Select ENSP00000225927.1:n.679-71T=
ENST00000225927.6:c.679-71T= ENSP00000225927.1:n.679-71T=
ENST00000586516.5:c.281-71T=
ENST00000591587.1:c.274-71T= ENSP00000467836.1:n.274-71T=
NM_000263.3:c.679-71T= NP_000254.2:n.679-71T=
XM_006721920.2:c.-64-71T= XP_006721983.1:n.-64-71T=
XM_011524840.1:c.-64-71T= XP_011523142.1:n.-64-71T=
XM_017024687.1:c.-64-71T= XP_016880176.1:n.-64-71T=
XM_024450771.1:c.736-71T= XP_024306539.1:n.736-71T=
XM_024450772.1:c.-64-71T= XP_024306540.1:n.-64-71T=
NM_000263.4:c.679-71T= MANE Select NP_000254.2:n.679-71T=