Canonical Allele Identifier: CA399595332
Gene: NAGLU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42536384C>G , CM000679.2:g.42536384C>G GRCh38
NC_000017.10:g.40688402C>G , CM000679.1:g.40688402C>G GRCh37
NC_000017.9:g.37941928C>G NCBI36
NG_011552.1:g.5452C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.112C>G MANE Select ENSP00000225927.1:p.Arg38Gly
ENST00000225927.6:c.112C>G ENSP00000225927.1:p.Arg38Gly
NM_000263.3:c.112C>G NP_000254.2:p.Arg38Gly
XM_024450771.1:c.112C>G XP_024306539.1:p.Arg38Gly
NM_000263.4:c.112C>G MANE Select NP_000254.2:p.Arg38Gly