Canonical Allele Identifier: CA1433072314
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1003642_1003645delinsGCCC , CM000666.2:g.1003642_1003645delinsGCCC GRCh38
NC_000004.11:g.997430_997433delinsGCCC , CM000666.1:g.997430_997433delinsGCCC GRCh37
NC_000004.10:g.987430_987433delinsGCCC NCBI36
NG_008103.1:g.21646_21649delinsGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.1727+17_1727+20delinsGCCC ENSP00000247933.4:n.1727+17_1727+20delinsGCCC
ENST00000514224.2:c.1727+17_1727+20delinsGCCC MANE Select ENSP00000425081.2:n.1727+17_1727+20delinsGCCC
ENST00000652070.1:n.1783+17_1783+20delinsGCCC
ENST00000247933.8:c.1727+17_1727+20delinsGCCC ENSP00000247933.4:n.1727+17_1727+20delinsGCCC
ENST00000514224.1:c.1331+17_1331+20delinsGCCC ENSP00000425081.1:n.1331+17_1331+20delinsGCCC
ENST00000514417.1:n.136_139delinsGCCC
ENST00000514698.5:n.1838+13_1838+16delinsGCCC
NM_000203.4:c.1727+17_1727+20delinsGCCC NP_000194.2:n.1727+17_1727+20delinsGCCC
NR_110313.1:n.1819+13_1819+16delinsGCCC
XM_006713882.2:c.1331+17_1331+20delinsGCCC XP_006713945.1:n.1331+17_1331+20delinsGCCC
XM_011513459.1:c.1793+17_1793+20delinsGCCC XP_011511761.1:n.1793+17_1793+20delinsGCCC
XM_011513460.1:c.1586+17_1586+20delinsGCCC XP_011511762.1:n.1586+17_1586+20delinsGCCC
XM_011513461.1:c.1520+17_1520+20delinsGCCC XP_011511763.1:n.1520+17_1520+20delinsGCCC
XM_011513462.1:c.1439+17_1439+20delinsGCCC XP_011511764.1:n.1439+17_1439+20delinsGCCC
XM_011513463.1:c.1439+17_1439+20delinsGCCC XP_011511765.1:n.1439+17_1439+20delinsGCCC
XR_924947.1:n.1987+13_1987+16delinsGCCC
NM_000203.5:c.1727+17_1727+20delinsGCCC MANE Select NP_000194.2:n.1727+17_1727+20delinsGCCC
NM_001363576.1:c.1331+17_1331+20delinsGCCC NP_001350505.1:n.1331+17_1331+20delinsGCCC
XM_011513461.2:c.1520+17_1520+20delinsGCCC XP_011511763.1:n.1520+17_1520+20delinsGCCC
XM_017008163.1:c.767+17_767+20delinsGCCC XP_016863652.1:n.767+17_767+20delinsGCCC