Canonical Allele Identifier: CA399605526
Gene: NAGLU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42543937A>T , CM000679.2:g.42543937A>T GRCh38
NC_000017.10:g.40695955A>T , CM000679.1:g.40695955A>T GRCh37
NC_000017.9:g.37949481A>T NCBI36
NG_011552.1:g.13005A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.1931A>T MANE Select ENSP00000225927.1:p.Tyr644Phe
ENST00000225927.6:c.1931A>T ENSP00000225927.1:p.Tyr644Phe
ENST00000591587.1:c.1269A>T ENSP00000467836.1:n.1269A>T
NM_000263.3:c.1931A>T NP_000254.2:p.Tyr644Phe
XM_006721920.2:c.1100A>T XP_006721983.1:p.Tyr367Phe
XM_011524840.1:c.932A>T XP_011523142.1:p.Tyr311Phe
XM_017024687.1:c.1100A>T XP_016880176.1:p.Tyr367Phe
XM_024450771.1:c.1988A>T XP_024306539.1:p.Tyr663Phe
XM_024450772.1:c.932A>T XP_024306540.1:p.Tyr311Phe
NM_000263.4:c.1931A>T MANE Select NP_000254.2:p.Tyr644Phe