Canonical Allele Identifier: CA2637969887
Gene: NAGLU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42538598A>G , CM000679.2:g.42538598A>G GRCh38
NC_000017.10:g.40690616A>G , CM000679.1:g.40690616A>G GRCh37
NC_000017.9:g.37944142A>G NCBI36
NG_011552.1:g.7666A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.679-72A>G MANE Select ENSP00000225927.1:n.679-72A>G
ENST00000225927.6:c.679-72A>G ENSP00000225927.1:n.679-72A>G
ENST00000586516.5:c.281-72A>G
ENST00000591587.1:c.274-72A>G ENSP00000467836.1:n.274-72A>G
NM_000263.3:c.679-72A>G NP_000254.2:n.679-72A>G
XM_006721920.2:c.-64-72A>G XP_006721983.1:n.-64-72A>G
XM_011524840.1:c.-64-72A>G XP_011523142.1:n.-64-72A>G
XM_017024687.1:c.-64-72A>G XP_016880176.1:n.-64-72A>G
XM_024450771.1:c.736-72A>G XP_024306539.1:n.736-72A>G
XM_024450772.1:c.-64-72A>G XP_024306540.1:n.-64-72A>G
NM_000263.4:c.679-72A>G MANE Select NP_000254.2:n.679-72A>G