Canonical Allele Identifier: CA399598793
Community Standard Title: NM_000263.4(NAGLU):c.676C>T (p.Gln226Ter)
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42538483C>T , CM000679.2:g.42538483C>T GRCh38
NC_000017.10:g.40690501C>T , CM000679.1:g.40690501C>T GRCh37
NC_000017.9:g.37944027C>T NCBI36
NG_011552.1:g.7551C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000263.4:c.676C>T MANE Select NP_000254.2:p.Gln226Ter
ENST00000225927.7:c.676C>T MANE Select ENSP00000225927.1:p.Gln226Ter
NM_000263.3:c.676C>T NP_000254.2:p.Gln226Ter
ENST00000225927.6:c.676C>T ENSP00000225927.1:p.Gln226Ter
ENST00000586516.5:c.278C>T
ENST00000591587.1:c.271C>T ENSP00000467836.1:p.Gln91Ter
XM_006721920.2:c.-67C>T XP_006721983.1:n.-67C>T
XM_011524840.1:c.-67C>T XP_011523142.1:n.-67C>T
XM_017024687.1:c.-67C>T XP_016880176.1:n.-67C>T
XM_024450771.1:c.733C>T XP_024306539.1:p.Gln245Ter
XM_024450772.1:c.-67C>T XP_024306540.1:n.-67C>T