Canonical Allele Identifier: CA2669482880
Gene: IDUA HGNC NCBI

Linked Data

gnomAD v4: 4-1003321-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1003321C>T , CM000666.2:g.1003321C>T GRCh38
NC_000004.11:g.997109C>T , CM000666.1:g.997109C>T GRCh37
NC_000004.10:g.987109C>T NCBI36
NG_008103.1:g.21325C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000247933.9:c.1525-24C>T ENSP00000247933.4:n.1525-24C>T
ENST00000514224.2:c.1525-24C>T MANE Select ENSP00000425081.2:n.1525-24C>T
ENST00000652070.1:n.1581-24C>T
ENST00000247933.8:c.1525-24C>T ENSP00000247933.4:n.1525-24C>T
ENST00000502829.1:n.490C>T
ENST00000514224.1:c.1129-24C>T ENSP00000425081.1:n.1129-24C>T
ENST00000514698.5:n.1632-24C>T
NM_000203.4:c.1525-24C>T NP_000194.2:n.1525-24C>T
NR_110313.1:n.1613-24C>T
XM_006713882.2:c.1129-24C>T XP_006713945.1:n.1129-24C>T
XM_011513459.1:c.1591-24C>T XP_011511761.1:n.1591-24C>T
XM_011513460.1:c.1384-24C>T XP_011511762.1:n.1384-24C>T
XM_011513461.1:c.1318-24C>T XP_011511763.1:n.1318-24C>T
XM_011513462.1:c.1237-24C>T XP_011511764.1:n.1237-24C>T
XM_011513463.1:c.1237-24C>T XP_011511765.1:n.1237-24C>T
XR_924947.1:n.1757C>T
NM_000203.5:c.1525-24C>T MANE Select NP_000194.2:n.1525-24C>T
NM_001363576.1:c.1129-24C>T NP_001350505.1:n.1129-24C>T
XM_011513461.2:c.1318-24C>T XP_011511763.1:n.1318-24C>T
XM_017008163.1:c.565-24C>T XP_016863652.1:n.565-24C>T