Canonical Allele Identifier: CA2260529070
Gene: NAGLU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42540923A= , CM000679.2:g.42540923A= GRCh38
NC_000017.10:g.40692941A= , CM000679.1:g.40692941A= GRCh37
NC_000017.9:g.37946467A= NCBI36
NG_011552.1:g.9991A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225927.7:c.765-27A= MANE Select ENSP00000225927.1:n.765-27A=
ENST00000225927.6:c.765-27A= ENSP00000225927.1:n.765-27A=
ENST00000586516.5:c.367-27A=
ENST00000591587.1:c.360-2105A= ENSP00000467836.1:n.360-2105A=
NM_000263.3:c.765-27A= NP_000254.2:n.765-27A=
XM_006721920.2:c.23-116A= XP_006721983.1:n.23-116A=
XM_011524840.1:c.23-2105A= XP_011523142.1:n.23-2105A=
XM_017024687.1:c.23-116A= XP_016880176.1:n.23-116A=
XM_024450771.1:c.822-27A= XP_024306539.1:n.822-27A=
XM_024450772.1:c.23-2105A= XP_024306540.1:n.23-2105A=
NM_000263.4:c.765-27A= MANE Select NP_000254.2:n.765-27A=