Canonical Allele Identifier: CA399598506
Community Standard Title: NM_000263.4(NAGLU):c.603G>A (p.Trp201Ter)
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42538410G>A , CM000679.2:g.42538410G>A GRCh38
NC_000017.10:g.40690428G>A , CM000679.1:g.40690428G>A GRCh37
NC_000017.9:g.37943954G>A NCBI36
NG_011552.1:g.7478G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000263.4:c.603G>A MANE Select NP_000254.2:p.Trp201Ter
ENST00000225927.7:c.603G>A MANE Select ENSP00000225927.1:p.Trp201Ter
NM_000263.3:c.603G>A NP_000254.2:p.Trp201Ter
ENST00000225927.6:c.603G>A ENSP00000225927.1:p.Trp201Ter
ENST00000586516.5:c.205G>A
ENST00000591587.1:c.198G>A ENSP00000467836.1:p.Trp66Ter
XM_006721920.2:c.-140G>A XP_006721983.1:n.-140G>A
XM_011524840.1:c.-140G>A XP_011523142.1:n.-140G>A
XM_017024687.1:c.-140G>A XP_016880176.1:n.-140G>A
XM_024450771.1:c.660G>A XP_024306539.1:p.Trp220Ter
XM_024450772.1:c.-140G>A XP_024306540.1:n.-140G>A