Canonical Allele Identifier: CA1433071706
Gene: IDUA HGNC NCBI

Linked Data

dbSNP Id: rs1715232627
gnomAD v3: 4-1003319-C-A
gnomAD v4: 4-1003319-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1003319C>A , CM000666.2:g.1003319C>A GRCh38
NC_000004.11:g.997107C>A , CM000666.1:g.997107C>A GRCh37
NC_000004.10:g.987107C>A NCBI36
NG_008103.1:g.21323C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000247933.9:c.1525-26C>A ENSP00000247933.4:n.1525-26C>A
ENST00000514224.2:c.1525-26C>A MANE Select ENSP00000425081.2:n.1525-26C>A
ENST00000652070.1:n.1581-26C>A
ENST00000247933.8:c.1525-26C>A ENSP00000247933.4:n.1525-26C>A
ENST00000502829.1:n.488C>A
ENST00000514224.1:c.1129-26C>A ENSP00000425081.1:n.1129-26C>A
ENST00000514698.5:n.1632-26C>A
NM_000203.4:c.1525-26C>A NP_000194.2:n.1525-26C>A
NR_110313.1:n.1613-26C>A
XM_006713882.2:c.1129-26C>A XP_006713945.1:n.1129-26C>A
XM_011513459.1:c.1591-26C>A XP_011511761.1:n.1591-26C>A
XM_011513460.1:c.1384-26C>A XP_011511762.1:n.1384-26C>A
XM_011513461.1:c.1318-26C>A XP_011511763.1:n.1318-26C>A
XM_011513462.1:c.1237-26C>A XP_011511764.1:n.1237-26C>A
XM_011513463.1:c.1237-26C>A XP_011511765.1:n.1237-26C>A
XR_924947.1:n.1755C>A
NM_000203.5:c.1525-26C>A MANE Select NP_000194.2:n.1525-26C>A
NM_001363576.1:c.1129-26C>A NP_001350505.1:n.1129-26C>A
XM_011513461.2:c.1318-26C>A XP_011511763.1:n.1318-26C>A
XM_017008163.1:c.565-26C>A XP_016863652.1:n.565-26C>A