Canonical Allele Identifier: CA2260530670
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42544224G= , CM000679.2:g.42544224G= GRCh38
NC_000017.10:g.40696242G= , CM000679.1:g.40696242G= GRCh37
NC_000017.9:g.37949768G= NCBI36
NG_011552.1:g.13292G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.2218G= MANE Select ENSP00000225927.1:p.Ala740=
ENST00000225927.6:c.2218G= ENSP00000225927.1:p.Ala740=
NM_000263.3:c.2218G= NP_000254.2:p.Ala740=
XM_006721920.2:c.1387G= XP_006721983.1:p.Ala463=
XM_011524840.1:c.1219G= XP_011523142.1:p.Ala407=
XM_017024687.1:c.1387G= XP_016880176.1:p.Ala463=
XM_024450771.1:c.2275G= XP_024306539.1:p.Ala759=
XM_024450772.1:c.1219G= XP_024306540.1:p.Ala407=
NM_000263.4:c.2218G= MANE Select NP_000254.2:p.Ala740=