Canonical Allele Identifier: CA399605522
Gene: NAGLU HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000225927.7:c.1931A>C MANE Select ENSP00000225927.1:p.Tyr644Ser
ENST00000225927.6:c.1931A>C ENSP00000225927.1:p.Tyr644Ser
ENST00000591587.1:c.1269A>C ENSP00000467836.1:n.1269A>C
NM_000263.3:c.1931A>C NP_000254.2:p.Tyr644Ser
XM_006721920.2:c.1100A>C XP_006721983.1:p.Tyr367Ser
XM_011524840.1:c.932A>C XP_011523142.1:p.Tyr311Ser
XM_017024687.1:c.1100A>C XP_016880176.1:p.Tyr367Ser
XM_024450771.1:c.1988A>C XP_024306539.1:p.Tyr663Ser
XM_024450772.1:c.932A>C XP_024306540.1:p.Tyr311Ser
NM_000263.4:c.1931A>C MANE Select NP_000254.2:p.Tyr644Ser