Canonical Allele Identifier: CA399601403
Community Standard Title: NM_000263.4(NAGLU):c.1199A>C (p.Gln400Pro)
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42543205A>C , CM000679.2:g.42543205A>C GRCh38
NC_000017.10:g.40695223A>C , CM000679.1:g.40695223A>C GRCh37
NC_000017.9:g.37948749A>C NCBI36
NG_011552.1:g.12273A>C

Transcript Alleles

HGVS Amino-acid Change
NM_000263.4:c.1199A>C MANE Select NP_000254.2:p.Gln400Pro
ENST00000225927.7:c.1199A>C MANE Select ENSP00000225927.1:p.Gln400Pro
NM_000263.3:c.1199A>C NP_000254.2:p.Gln400Pro
ENST00000225927.6:c.1199A>C ENSP00000225927.1:p.Gln400Pro
ENST00000591587.1:c.537A>C ENSP00000467836.1:n.537A>C
ENST00000592454.1:c.238A>C
XM_006721920.2:c.368A>C XP_006721983.1:p.Gln123Pro
XM_011524840.1:c.200A>C XP_011523142.1:p.Gln67Pro
XM_017024687.1:c.368A>C XP_016880176.1:p.Gln123Pro
XM_024450771.1:c.1256A>C XP_024306539.1:p.Gln419Pro
XM_024450772.1:c.200A>C XP_024306540.1:p.Gln67Pro