Canonical Allele Identifier: CA355965005
Gene: IDUA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1003403C>G , CM000666.2:g.1003403C>G GRCh38
NC_000004.11:g.997191C>G , CM000666.1:g.997191C>G GRCh37
NC_000004.10:g.987191C>G NCBI36
NG_008103.1:g.21407C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.1583C>G ENSP00000247933.4:p.Pro528Arg
ENST00000514224.2:c.1583C>G MANE Select ENSP00000425081.2:p.Pro528Arg
ENST00000652070.1:n.1639C>G
ENST00000247933.8:c.1583C>G ENSP00000247933.4:p.Pro528Arg
ENST00000514224.1:c.1187C>G ENSP00000425081.1:p.Pro396Arg
ENST00000514698.5:n.1690C>G
NM_000203.4:c.1583C>G NP_000194.2:p.Pro528Arg
NR_110313.1:n.1671C>G
XM_006713882.2:c.1187C>G XP_006713945.1:p.Pro396Arg
XM_011513459.1:c.1649C>G XP_011511761.1:p.Pro550Arg
XM_011513460.1:c.1442C>G XP_011511762.1:p.Pro481Arg
XM_011513461.1:c.1376C>G XP_011511763.1:p.Pro459Arg
XM_011513462.1:c.1295C>G XP_011511764.1:p.Pro432Arg
XM_011513463.1:c.1295C>G XP_011511765.1:p.Pro432Arg
XR_924947.1:n.1839C>G
NM_000203.5:c.1583C>G MANE Select NP_000194.2:p.Pro528Arg
NM_001363576.1:c.1187C>G NP_001350505.1:p.Pro396Arg
XM_011513461.2:c.1376C>G XP_011511763.1:p.Pro459Arg
XM_017008163.1:c.623C>G XP_016863652.1:p.Pro208Arg