Canonical Allele Identifier: CA8576757
Community Standard Title: NM_000263.4(NAGLU):c.384-1G>A
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42537397G>A , CM000679.2:g.42537397G>A GRCh38
NC_000017.10:g.40689415G>A , CM000679.1:g.40689415G>A GRCh37
NC_000017.9:g.37942941G>A NCBI36
NG_011552.1:g.6465G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000263.4:c.384-1G>A MANE Select NP_000254.2:n.384-1G>A
ENST00000225927.7:c.384-1G>A MANE Select ENSP00000225927.1:n.384-1G>A
NM_000263.3:c.384-1G>A NP_000254.2:n.384-1G>A
ENST00000225927.6:c.384-1G>A ENSP00000225927.1:n.384-1G>A
ENST00000586516.5:c.133+742G>A
ENST00000590358.1:c.71G>A ENSP00000466892.1:p.Arg24Lys
ENST00000591587.1:c.126+742G>A ENSP00000467836.1:n.126+742G>A
XM_006721920.2:c.-359-1G>A XP_006721983.1:n.-359-1G>A
XM_011524840.1:c.-359-1G>A XP_011523142.1:n.-359-1G>A
XM_017024687.1:c.-360G>A XP_016880176.1:n.-360G>A
XM_024450771.1:c.441-1G>A XP_024306539.1:n.441-1G>A
XM_024450772.1:c.-360G>A XP_024306540.1:n.-360G>A