Canonical Allele Identifier: CA2760125568
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002220del , CM000666.2:g.1002220del GRCh38
NC_000004.11:g.996008del , CM000666.1:g.996008del GRCh37
NC_000004.10:g.986008del NCBI36
NG_008103.1:g.20224del

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.973-49del ENSP00000247933.4:n.973-49del
ENST00000514224.2:c.973-49del MANE Select ENSP00000425081.2:n.973-49del
ENST00000652070.1:n.1029-49del
ENST00000247933.8:c.973-49del ENSP00000247933.4:n.973-49del
ENST00000514224.1:c.577-49del ENSP00000425081.1:n.577-49del
ENST00000514698.5:n.1031del
NM_000203.4:c.973-49del NP_000194.2:n.973-49del
NR_110313.1:n.1061-49del
XM_006713882.2:c.577-49del XP_006713945.1:n.577-49del
XM_011513459.1:c.990del XP_011511761.1:p.Arg330SerfsTer?
XM_011513460.1:c.832-49del XP_011511762.1:n.832-49del
XM_011513461.1:c.766-49del XP_011511763.1:n.766-49del
XM_011513462.1:c.685-49del XP_011511764.1:n.685-49del
XM_011513463.1:c.685-49del XP_011511765.1:n.685-49del
XR_924947.1:n.1042-49del
NM_000203.5:c.973-49del MANE Select NP_000194.2:n.973-49del
NM_001363576.1:c.577-49del NP_001350505.1:n.577-49del
XM_011513461.2:c.766-49del XP_011511763.1:n.766-49del
XM_017008163.1:c.13-49del XP_016863652.1:n.13-49del