Canonical Allele Identifier: CA2802202
Community Standard Title: NM_000203.5(IDUA):c.1139A>G (p.Gln380Arg)
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002435A>G , CM000666.2:g.1002435A>G GRCh38
NC_000004.11:g.996223A>G , CM000666.1:g.996223A>G GRCh37
NC_000004.10:g.986223A>G NCBI36
NG_008103.1:g.20439A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000203.5:c.1139A>G MANE Select NP_000194.2:p.Gln380Arg
ENST00000514224.2:c.1139A>G MANE Select ENSP00000425081.2:p.Gln380Arg
NM_000203.4:c.1139A>G NP_000194.2:p.Gln380Arg
NM_001363576.1:c.743A>G NP_001350505.1:p.Gln248Arg
NR_110313.1:n.1227A>G
ENST00000247933.8:c.1139A>G ENSP00000247933.4:p.Gln380Arg
ENST00000247933.9:c.1139A>G ENSP00000247933.4:p.Gln380Arg
ENST00000514224.1:c.743A>G ENSP00000425081.1:p.Gln248Arg
ENST00000514698.5:n.1246A>G
ENST00000652070.1:n.1195A>G
XM_006713882.2:c.743A>G XP_006713945.1:p.Gln248Arg
XM_011513459.1:c.1205A>G XP_011511761.1:p.Gln402Arg
XM_011513460.1:c.998A>G XP_011511762.1:p.Gln333Arg
XM_011513461.1:c.932A>G XP_011511763.1:p.Gln311Arg
XM_011513461.2:c.932A>G XP_011511763.1:p.Gln311Arg
XM_011513462.1:c.851A>G XP_011511764.1:p.Gln284Arg
XM_011513463.1:c.851A>G XP_011511765.1:p.Gln284Arg
XM_017008163.1:c.179A>G XP_016863652.1:p.Gln60Arg
XR_924947.1:n.1208A>G