Canonical Allele Identifier: CA2260526803
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536532C= , CM000679.2:g.42536532C= GRCh38
NC_000017.10:g.40688550C= , CM000679.1:g.40688550C= GRCh37
NC_000017.9:g.37942076C= NCBI36
NG_011552.1:g.5600C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.260C= MANE Select ENSP00000225927.1:p.Ala87=
ENST00000225927.6:c.260C= ENSP00000225927.1:p.Ala87=
ENST00000586516.5:c.10C=
ENST00000591587.1:c.3C= ENSP00000467836.1:p.Arg1=
NM_000263.3:c.260C= NP_000254.2:p.Ala87=
XM_024450771.1:c.260C= XP_024306539.1:p.Ala87=
NM_000263.4:c.260C= MANE Select NP_000254.2:p.Ala87=