Canonical Allele Identifier: CA1433067449
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1001544C= , CM000666.2:g.1001544C= GRCh38
NC_000004.11:g.995332C= , CM000666.1:g.995332C= GRCh37
NC_000004.10:g.985332C= NCBI36
NG_008103.1:g.19548C=

Transcript Alleles

HGVS Amino-acid change
ENST00000247933.9:c.570C= ENSP00000247933.4:p.Asn190=
ENST00000514224.2:c.570C= MANE Select ENSP00000425081.2:p.Asn190=
ENST00000652070.1:n.626C=
ENST00000247933.8:c.570C= ENSP00000247933.4:p.Asn190=
ENST00000502910.5:c.429C= ENSP00000422952.1:p.Asn143=
ENST00000504568.5:c.530C=
ENST00000509948.5:c.363C= ENSP00000424227.1:p.Asn121=
ENST00000514192.5:c.387C= ENSP00000423685.1:p.Asn129=
ENST00000514224.1:c.174C= ENSP00000425081.1:p.Asn58=
ENST00000514698.5:n.470C=
NM_000203.4:c.570C= NP_000194.2:p.Asn190=
NR_110313.1:n.658C=
XM_006713882.2:c.174C= XP_006713945.1:p.Asn58=
XM_011513459.1:c.429C= XP_011511761.1:p.Asn143=
XM_011513460.1:c.429C= XP_011511762.1:p.Asn143=
XM_011513461.1:c.363C= XP_011511763.1:p.Asn121=
XM_011513462.1:c.282C= XP_011511764.1:p.Asn94=
XM_011513463.1:c.282C= XP_011511765.1:p.Asn94=
XR_924947.1:n.639C=
NM_000203.5:c.570C= MANE Select NP_000194.2:p.Asn190=
NM_001363576.1:c.174C= NP_001350505.1:p.Asn58=
XM_011513461.2:c.363C= XP_011511763.1:p.Asn121=
XM_017008163.1:c.-419C= XP_016863652.1:n.-419C=