Canonical Allele Identifier: CA2669480667
Gene: IDUA HGNC NCBI

Linked Data

gnomAD v4: 4-1001340-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1001340A>G , CM000666.2:g.1001340A>G GRCh38
NC_000004.11:g.995128A>G , CM000666.1:g.995128A>G GRCh37
NC_000004.10:g.985128A>G NCBI36
NG_008103.1:g.19344A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.494-128A>G ENSP00000247933.4:n.494-128A>G
ENST00000514224.2:c.494-128A>G MANE Select ENSP00000425081.2:n.494-128A>G
ENST00000652070.1:n.550-128A>G
ENST00000247933.8:c.494-128A>G ENSP00000247933.4:n.494-128A>G
ENST00000502910.5:c.353-128A>G ENSP00000422952.1:n.353-128A>G
ENST00000504568.5:c.454-128A>G
ENST00000509948.5:c.287-128A>G ENSP00000424227.1:n.287-128A>G
ENST00000514192.5:c.311-128A>G ENSP00000423685.1:n.311-128A>G
ENST00000514224.1:c.98-128A>G ENSP00000425081.1:n.98-128A>G
ENST00000514698.5:n.394-128A>G
NM_000203.4:c.494-128A>G NP_000194.2:n.494-128A>G
NR_110313.1:n.582-128A>G
XM_006713882.2:c.98-128A>G XP_006713945.1:n.98-128A>G
XM_011513459.1:c.353-128A>G XP_011511761.1:n.353-128A>G
XM_011513460.1:c.353-128A>G XP_011511762.1:n.353-128A>G
XM_011513461.1:c.287-128A>G XP_011511763.1:n.287-128A>G
XM_011513462.1:c.206-128A>G XP_011511764.1:n.206-128A>G
XM_011513463.1:c.206-128A>G XP_011511765.1:n.206-128A>G
XR_924947.1:n.563-128A>G
NM_000203.5:c.494-128A>G MANE Select NP_000194.2:n.494-128A>G
NM_001363576.1:c.98-128A>G NP_001350505.1:n.98-128A>G
XM_011513461.2:c.287-128A>G XP_011511763.1:n.287-128A>G
XM_017008163.1:c.-623A>G XP_016863652.1:n.-623A>G