Canonical Allele Identifier: CA1433068301
Gene: IDUA HGNC NCBI

Linked Data

dbSNP Id: rs1715108084

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1001937dup , CM000666.2:g.1001937dup GRCh38
NC_000004.11:g.995725dup , CM000666.1:g.995725dup GRCh37
NC_000004.10:g.985725dup NCBI36
NG_008103.1:g.19941dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.793-45dup ENSP00000247933.4:n.793-45dup
ENST00000514224.2:c.793-45dup MANE Select ENSP00000425081.2:n.793-45dup
ENST00000652070.1:n.849-45dup
ENST00000247933.8:c.793-45dup ENSP00000247933.4:n.793-45dup
ENST00000502910.5:c.652-45dup ENSP00000422952.1:n.652-45dup
ENST00000514192.5:c.610-45dup ENSP00000423685.1:n.610-45dup
ENST00000514224.1:c.397-45dup ENSP00000425081.1:n.397-45dup
ENST00000514698.5:n.748dup
NM_000203.4:c.793-45dup NP_000194.2:n.793-45dup
NR_110313.1:n.881-45dup
XM_006713882.2:c.397-45dup XP_006713945.1:n.397-45dup
XM_011513459.1:c.707dup XP_011511761.1:p.Arg238ProfsTer3
XM_011513460.1:c.652-45dup XP_011511762.1:n.652-45dup
XM_011513461.1:c.586-45dup XP_011511763.1:n.586-45dup
XM_011513462.1:c.505-45dup XP_011511764.1:n.505-45dup
XM_011513463.1:c.505-45dup XP_011511765.1:n.505-45dup
XR_924947.1:n.862-45dup
NM_000203.5:c.793-45dup MANE Select NP_000194.2:n.793-45dup
NM_001363576.1:c.397-45dup NP_001350505.1:n.397-45dup
XM_011513461.2:c.586-45dup XP_011511763.1:n.586-45dup
XM_017008163.1:c.-168-45dup XP_016863652.1:n.-168-45dup