Canonical Allele Identifier: CA2669480148
Gene: IDUA HGNC NCBI

Linked Data

gnomAD v4: 4-1001918-GC-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1001921del , CM000666.2:g.1001921del GRCh38
NC_000004.11:g.995709del , CM000666.1:g.995709del GRCh37
NC_000004.10:g.985709del NCBI36
NG_008103.1:g.19925del

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.792+40del ENSP00000247933.4:n.792+40del
ENST00000514224.2:c.792+40del MANE Select ENSP00000425081.2:n.792+40del
ENST00000652070.1:n.848+40del
ENST00000247933.8:c.792+40del ENSP00000247933.4:n.792+40del
ENST00000502910.5:c.651+40del ENSP00000422952.1:n.651+40del
ENST00000514192.5:c.609+40del ENSP00000423685.1:n.609+40del
ENST00000514224.1:c.396+40del ENSP00000425081.1:n.396+40del
ENST00000514698.5:n.732del
NM_000203.4:c.792+40del NP_000194.2:n.792+40del
NR_110313.1:n.880+40del
XM_006713882.2:c.396+40del XP_006713945.1:n.396+40del
XM_011513459.1:c.691del XP_011511761.1:p.Leu231SerfsTer?
XM_011513460.1:c.651+40del XP_011511762.1:n.651+40del
XM_011513461.1:c.585+40del XP_011511763.1:n.585+40del
XM_011513462.1:c.504+40del XP_011511764.1:n.504+40del
XM_011513463.1:c.504+40del XP_011511765.1:n.504+40del
XR_924947.1:n.861+40del
NM_000203.5:c.792+40del MANE Select NP_000194.2:n.792+40del
NM_001363576.1:c.396+40del NP_001350505.1:n.396+40del
XM_011513461.2:c.585+40del XP_011511763.1:n.585+40del
XM_017008163.1:c.-169+40del XP_016863652.1:n.-169+40del