Canonical Allele Identifier: CA399605110
Gene: NAGLU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42543853T>G , CM000679.2:g.42543853T>G GRCh38
NC_000017.10:g.40695871T>G , CM000679.1:g.40695871T>G GRCh37
NC_000017.9:g.37949397T>G NCBI36
NG_011552.1:g.12921T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000225927.7:c.1847T>G MANE Select ENSP00000225927.1:p.Phe616Cys
ENST00000225927.6:c.1847T>G ENSP00000225927.1:p.Phe616Cys
ENST00000591587.1:c.1185T>G ENSP00000467836.1:n.1185T>G
NM_000263.3:c.1847T>G NP_000254.2:p.Phe616Cys
XM_006721920.2:c.1016T>G XP_006721983.1:p.Phe339Cys
XM_011524840.1:c.848T>G XP_011523142.1:p.Phe283Cys
XM_017024687.1:c.1016T>G XP_016880176.1:p.Phe339Cys
XM_024450771.1:c.1904T>G XP_024306539.1:p.Phe635Cys
XM_024450772.1:c.848T>G XP_024306540.1:p.Phe283Cys
NM_000263.4:c.1847T>G MANE Select NP_000254.2:p.Phe616Cys