Canonical Allele Identifier: CA1433067413
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1001528A= , CM000666.2:g.1001528A= GRCh38
NC_000004.11:g.995316A= , CM000666.1:g.995316A= GRCh37
NC_000004.10:g.985316A= NCBI36
NG_008103.1:g.19532A=

Transcript Alleles

HGVS Amino-acid change
ENST00000247933.9:c.554A= ENSP00000247933.4:p.His185=
ENST00000514224.2:c.554A= MANE Select ENSP00000425081.2:p.His185=
ENST00000652070.1:n.610A=
ENST00000247933.8:c.554A= ENSP00000247933.4:p.His185=
ENST00000502910.5:c.413A= ENSP00000422952.1:p.His138=
ENST00000504568.5:c.514A=
ENST00000509948.5:c.347A= ENSP00000424227.1:p.His116=
ENST00000514192.5:c.371A= ENSP00000423685.1:p.His124=
ENST00000514224.1:c.158A= ENSP00000425081.1:p.His53=
ENST00000514698.5:n.454A=
NM_000203.4:c.554A= NP_000194.2:p.His185=
NR_110313.1:n.642A=
XM_006713882.2:c.158A= XP_006713945.1:p.His53=
XM_011513459.1:c.413A= XP_011511761.1:p.His138=
XM_011513460.1:c.413A= XP_011511762.1:p.His138=
XM_011513461.1:c.347A= XP_011511763.1:p.His116=
XM_011513462.1:c.266A= XP_011511764.1:p.His89=
XM_011513463.1:c.266A= XP_011511765.1:p.His89=
XR_924947.1:n.623A=
NM_000203.5:c.554A= MANE Select NP_000194.2:p.His185=
NM_001363576.1:c.158A= NP_001350505.1:p.His53=
XM_011513461.2:c.347A= XP_011511763.1:p.His116=
XM_017008163.1:c.-435A= XP_016863652.1:n.-435A=