Canonical Allele Identifier: CA399600777
Community Standard Title: NM_000263.4(NAGLU):c.1022-2A>G
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42543026A>G , CM000679.2:g.42543026A>G GRCh38
NC_000017.10:g.40695044A>G , CM000679.1:g.40695044A>G GRCh37
NC_000017.9:g.37948570A>G NCBI36
NG_011552.1:g.12094A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000263.4:c.1022-2A>G MANE Select NP_000254.2:n.1022-2A>G
ENST00000225927.7:c.1022-2A>G MANE Select ENSP00000225927.1:n.1022-2A>G
NM_000263.3:c.1022-2A>G NP_000254.2:n.1022-2A>G
ENST00000225927.6:c.1022-2A>G ENSP00000225927.1:n.1022-2A>G
ENST00000591587.1:c.360-2A>G ENSP00000467836.1:n.360-2A>G
ENST00000592454.1:c.117-58A>G
XM_006721920.2:c.191-2A>G XP_006721983.1:n.191-2A>G
XM_011524840.1:c.23-2A>G XP_011523142.1:n.23-2A>G
XM_017024687.1:c.191-2A>G XP_016880176.1:n.191-2A>G
XM_024450771.1:c.1079-2A>G XP_024306539.1:n.1079-2A>G
XM_024450772.1:c.23-2A>G XP_024306540.1:n.23-2A>G