Canonical Allele Identifier: CA399605559
Gene: NAGLU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42543946C>G , CM000679.2:g.42543946C>G GRCh38
NC_000017.10:g.40695964C>G , CM000679.1:g.40695964C>G GRCh37
NC_000017.9:g.37949490C>G NCBI36
NG_011552.1:g.13014C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.1940C>G MANE Select ENSP00000225927.1:p.Thr647Ser
ENST00000225927.6:c.1940C>G ENSP00000225927.1:p.Thr647Ser
ENST00000591587.1:c.1278C>G ENSP00000467836.1:n.1278C>G
NM_000263.3:c.1940C>G NP_000254.2:p.Thr647Ser
XM_006721920.2:c.1109C>G XP_006721983.1:p.Thr370Ser
XM_011524840.1:c.941C>G XP_011523142.1:p.Thr314Ser
XM_017024687.1:c.1109C>G XP_016880176.1:p.Thr370Ser
XM_024450771.1:c.1997C>G XP_024306539.1:p.Thr666Ser
XM_024450772.1:c.941C>G XP_024306540.1:p.Thr314Ser
NM_000263.4:c.1940C>G MANE Select NP_000254.2:p.Thr647Ser