Canonical Allele Identifier: CA2578014081
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1003229dup , CM000666.2:g.1003229dup GRCh38
NC_000004.11:g.997017dup , CM000666.1:g.997017dup GRCh37
NC_000004.10:g.987017dup NCBI36
NG_008103.1:g.21233dup

Transcript Alleles

HGVS Amino-acid change
ENST00000247933.9:c.1524+72dup ENSP00000247933.4:n.1524+72dup
ENST00000514224.2:c.1524+72dup MANE Select ENSP00000425081.2:n.1524+72dup
ENST00000652070.1:n.1580+72dup
ENST00000247933.8:c.1524+72dup ENSP00000247933.4:n.1524+72dup
ENST00000502829.1:n.398dup
ENST00000514224.1:c.1128+72dup ENSP00000425081.1:n.1128+72dup
ENST00000514698.5:n.1631+72dup
NM_000203.4:c.1524+72dup NP_000194.2:n.1524+72dup
NR_110313.1:n.1612+72dup
XM_006713882.2:c.1128+72dup XP_006713945.1:n.1128+72dup
XM_011513459.1:c.1590+72dup XP_011511761.1:n.1590+72dup
XM_011513460.1:c.1383+72dup XP_011511762.1:n.1383+72dup
XM_011513461.1:c.1317+72dup XP_011511763.1:n.1317+72dup
XM_011513462.1:c.1236+72dup XP_011511764.1:n.1236+72dup
XM_011513463.1:c.1236+72dup XP_011511765.1:n.1236+72dup
XR_924947.1:n.1665dup
NM_000203.5:c.1524+72dup MANE Select NP_000194.2:n.1524+72dup
NM_001363576.1:c.1128+72dup NP_001350505.1:n.1128+72dup
XM_011513461.2:c.1317+72dup XP_011511763.1:n.1317+72dup
XM_017008163.1:c.564+72dup XP_016863652.1:n.564+72dup