Canonical Allele Identifier: CA355963315
Community Standard Title: NM_000203.5(IDUA):c.1091C>A (p.Thr364Lys)
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002387C>A , CM000666.2:g.1002387C>A GRCh38
NC_000004.11:g.996175C>A , CM000666.1:g.996175C>A GRCh37
NC_000004.10:g.986175C>A NCBI36
NG_008103.1:g.20391C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000203.5:c.1091C>A MANE Select NP_000194.2:p.Thr364Lys
ENST00000514224.2:c.1091C>A MANE Select ENSP00000425081.2:p.Thr364Lys
NM_000203.4:c.1091C>A NP_000194.2:p.Thr364Lys
NM_001363576.1:c.695C>A NP_001350505.1:p.Thr232Lys
NR_110313.1:n.1179C>A
ENST00000247933.8:c.1091C>A ENSP00000247933.4:p.Thr364Lys
ENST00000247933.9:c.1091C>A ENSP00000247933.4:p.Thr364Lys
ENST00000514224.1:c.695C>A ENSP00000425081.1:p.Thr232Lys
ENST00000514698.5:n.1198C>A
ENST00000652070.1:n.1147C>A
XM_006713882.2:c.695C>A XP_006713945.1:p.Thr232Lys
XM_011513459.1:c.1157C>A XP_011511761.1:p.Thr386Lys
XM_011513460.1:c.950C>A XP_011511762.1:p.Thr317Lys
XM_011513461.1:c.884C>A XP_011511763.1:p.Thr295Lys
XM_011513461.2:c.884C>A XP_011511763.1:p.Thr295Lys
XM_011513462.1:c.803C>A XP_011511764.1:p.Thr268Lys
XM_011513463.1:c.803C>A XP_011511765.1:p.Thr268Lys
XM_017008163.1:c.131C>A XP_016863652.1:p.Thr44Lys
XR_924947.1:n.1160C>A