Canonical Allele Identifier: CA355963316

Gene: IDUA

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_000203.5:c.1091C>G MANE Select	NP_000194.2:p.Thr364Arg
ENST00000514224.2:c.1091C>G MANE Select	ENSP00000425081.2:p.Thr364Arg
NM_000203.4:c.1091C>G	NP_000194.2:p.Thr364Arg
NM_001363576.1:c.695C>G	NP_001350505.1:p.Thr232Arg
NR_110313.1:n.1179C>G
ENST00000247933.8:c.1091C>G	ENSP00000247933.4:p.Thr364Arg
ENST00000247933.9:c.1091C>G	ENSP00000247933.4:p.Thr364Arg
ENST00000514224.1:c.695C>G	ENSP00000425081.1:p.Thr232Arg
ENST00000514698.5:n.1198C>G
ENST00000652070.1:n.1147C>G
XM_006713882.2:c.695C>G	XP_006713945.1:p.Thr232Arg
XM_011513459.1:c.1157C>G	XP_011511761.1:p.Thr386Arg
XM_011513460.1:c.950C>G	XP_011511762.1:p.Thr317Arg
XM_011513461.1:c.884C>G	XP_011511763.1:p.Thr295Arg
XM_011513461.2:c.884C>G	XP_011511763.1:p.Thr295Arg
XM_011513462.1:c.803C>G	XP_011511764.1:p.Thr268Arg
XM_011513463.1:c.803C>G	XP_011511765.1:p.Thr268Arg
XM_017008163.1:c.131C>G	XP_016863652.1:p.Thr44Arg
XR_924947.1:n.1160C>G