Canonical Allele Identifier: CA2669482207
Gene: IDUA HGNC NCBI

Linked Data

gnomAD v4: 4-1002704-GC-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002705del , CM000666.2:g.1002705del GRCh38
NC_000004.11:g.996493del , CM000666.1:g.996493del GRCh37
NC_000004.10:g.986493del NCBI36
NG_008103.1:g.20709del

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.1190-27del ENSP00000247933.4:n.1190-27del
ENST00000514224.2:c.1190-27del MANE Select ENSP00000425081.2:n.1190-27del
ENST00000652070.1:n.1246-27del
ENST00000247933.8:c.1190-27del ENSP00000247933.4:n.1190-27del
ENST00000514224.1:c.794-27del ENSP00000425081.1:n.794-27del
ENST00000514698.5:n.1297-27del
NM_000203.4:c.1190-27del NP_000194.2:n.1190-27del
NR_110313.1:n.1278-27del
XM_006713882.2:c.794-27del XP_006713945.1:n.794-27del
XM_011513459.1:c.1256-27del XP_011511761.1:n.1256-27del
XM_011513460.1:c.1049-27del XP_011511762.1:n.1049-27del
XM_011513461.1:c.983-27del XP_011511763.1:n.983-27del
XM_011513462.1:c.902-27del XP_011511764.1:n.902-27del
XM_011513463.1:c.902-27del XP_011511765.1:n.902-27del
XR_924947.1:n.1259-27del
NM_000203.5:c.1190-27del MANE Select NP_000194.2:n.1190-27del
NM_001363576.1:c.794-27del NP_001350505.1:n.794-27del
XM_011513461.2:c.983-27del XP_011511763.1:n.983-27del
XM_017008163.1:c.230-27del XP_016863652.1:n.230-27del