Canonical Allele Identifier: CA355961928

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001703G>A , CM000666.2:g.1001703G>A	GRCh38
NC_000004.11:g.995491G>A , CM000666.1:g.995491G>A	GRCh37
NC_000004.10:g.985491G>A	NCBI36
NG_008103.1:g.19707G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000203.5:c.614G>A MANE Select	NP_000194.2:p.Cys205Tyr
ENST00000514224.2:c.614G>A MANE Select	ENSP00000425081.2:p.Cys205Tyr
NM_000203.4:c.614G>A	NP_000194.2:p.Cys205Tyr
NM_001363576.1:c.218G>A	NP_001350505.1:p.Cys73Tyr
NR_110313.1:n.702G>A
ENST00000247933.8:c.614G>A	ENSP00000247933.4:p.Cys205Tyr
ENST00000247933.9:c.614G>A	ENSP00000247933.4:p.Cys205Tyr
ENST00000502910.5:c.473G>A	ENSP00000422952.1:p.Cys158Tyr
ENST00000504568.5:c.574G>A
ENST00000509948.5:c.407G>A	ENSP00000424227.1:p.Cys136Tyr
ENST00000514192.5:c.431G>A	ENSP00000423685.1:p.Cys144Tyr
ENST00000514224.1:c.218G>A	ENSP00000425081.1:p.Cys73Tyr
ENST00000514698.5:n.514G>A
ENST00000652070.1:n.670G>A
XM_006713882.2:c.218G>A	XP_006713945.1:p.Cys73Tyr
XM_011513459.1:c.473G>A	XP_011511761.1:p.Cys158Tyr
XM_011513460.1:c.473G>A	XP_011511762.1:p.Cys158Tyr
XM_011513461.1:c.407G>A	XP_011511763.1:p.Cys136Tyr
XM_011513461.2:c.407G>A	XP_011511763.1:p.Cys136Tyr
XM_011513462.1:c.326G>A	XP_011511764.1:p.Cys109Tyr
XM_011513463.1:c.326G>A	XP_011511765.1:p.Cys109Tyr
XM_017008163.1:c.-347G>A	XP_016863652.1:n.-347G>A
XR_924947.1:n.683G>A