Canonical Allele Identifier: CA2578014073
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1003216dup , CM000666.2:g.1003216dup GRCh38
NC_000004.11:g.997004dup , CM000666.1:g.997004dup GRCh37
NC_000004.10:g.987004dup NCBI36
NG_008103.1:g.21220dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.1524+59dup ENSP00000247933.4:n.1524+59dup
ENST00000514224.2:c.1524+59dup MANE Select ENSP00000425081.2:n.1524+59dup
ENST00000652070.1:n.1580+59dup
ENST00000247933.8:c.1524+59dup ENSP00000247933.4:n.1524+59dup
ENST00000502829.1:n.385dup
ENST00000514224.1:c.1128+59dup ENSP00000425081.1:n.1128+59dup
ENST00000514698.5:n.1631+59dup
NM_000203.4:c.1524+59dup NP_000194.2:n.1524+59dup
NR_110313.1:n.1612+59dup
XM_006713882.2:c.1128+59dup XP_006713945.1:n.1128+59dup
XM_011513459.1:c.1590+59dup XP_011511761.1:n.1590+59dup
XM_011513460.1:c.1383+59dup XP_011511762.1:n.1383+59dup
XM_011513461.1:c.1317+59dup XP_011511763.1:n.1317+59dup
XM_011513462.1:c.1236+59dup XP_011511764.1:n.1236+59dup
XM_011513463.1:c.1236+59dup XP_011511765.1:n.1236+59dup
XR_924947.1:n.1652dup
NM_000203.5:c.1524+59dup MANE Select NP_000194.2:n.1524+59dup
NM_001363576.1:c.1128+59dup NP_001350505.1:n.1128+59dup
XM_011513461.2:c.1317+59dup XP_011511763.1:n.1317+59dup
XM_017008163.1:c.564+59dup XP_016863652.1:n.564+59dup