Canonical Allele Identifier: CA2669482202
Gene: IDUA HGNC NCBI

Linked Data

gnomAD v4: 4-1002702-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002702A>G , CM000666.2:g.1002702A>G GRCh38
NC_000004.11:g.996490A>G , CM000666.1:g.996490A>G GRCh37
NC_000004.10:g.986490A>G NCBI36
NG_008103.1:g.20706A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.1190-30A>G ENSP00000247933.4:n.1190-30A>G
ENST00000514224.2:c.1190-30A>G MANE Select ENSP00000425081.2:n.1190-30A>G
ENST00000652070.1:n.1246-30A>G
ENST00000247933.8:c.1190-30A>G ENSP00000247933.4:n.1190-30A>G
ENST00000514224.1:c.794-30A>G ENSP00000425081.1:n.794-30A>G
ENST00000514698.5:n.1297-30A>G
NM_000203.4:c.1190-30A>G NP_000194.2:n.1190-30A>G
NR_110313.1:n.1278-30A>G
XM_006713882.2:c.794-30A>G XP_006713945.1:n.794-30A>G
XM_011513459.1:c.1256-30A>G XP_011511761.1:n.1256-30A>G
XM_011513460.1:c.1049-30A>G XP_011511762.1:n.1049-30A>G
XM_011513461.1:c.983-30A>G XP_011511763.1:n.983-30A>G
XM_011513462.1:c.902-30A>G XP_011511764.1:n.902-30A>G
XM_011513463.1:c.902-30A>G XP_011511765.1:n.902-30A>G
XR_924947.1:n.1259-30A>G
NM_000203.5:c.1190-30A>G MANE Select NP_000194.2:n.1190-30A>G
NM_001363576.1:c.794-30A>G NP_001350505.1:n.794-30A>G
XM_011513461.2:c.983-30A>G XP_011511763.1:n.983-30A>G
XM_017008163.1:c.230-30A>G XP_016863652.1:n.230-30A>G