Canonical Allele Identifier: CA355964784

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003146C>G , CM000666.2:g.1003146C>G	GRCh38
NC_000004.11:g.996934C>G , CM000666.1:g.996934C>G	GRCh37
NC_000004.10:g.986934C>G	NCBI36
NG_008103.1:g.21150C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000203.5:c.1513C>G MANE Select	NP_000194.2:p.Arg505Gly
ENST00000514224.2:c.1513C>G MANE Select	ENSP00000425081.2:p.Arg505Gly
NM_000203.4:c.1513C>G	NP_000194.2:p.Arg505Gly
NM_001363576.1:c.1117C>G	NP_001350505.1:p.Arg373Gly
NR_110313.1:n.1601C>G
ENST00000247933.8:c.1513C>G	ENSP00000247933.4:p.Arg505Gly
ENST00000247933.9:c.1513C>G	ENSP00000247933.4:p.Arg505Gly
ENST00000502829.1:n.315C>G
ENST00000514224.1:c.1117C>G	ENSP00000425081.1:p.Arg373Gly
ENST00000514698.5:n.1620C>G
ENST00000652070.1:n.1569C>G
XM_006713882.2:c.1117C>G	XP_006713945.1:p.Arg373Gly
XM_011513459.1:c.1579C>G	XP_011511761.1:p.Arg527Gly
XM_011513460.1:c.1372C>G	XP_011511762.1:p.Arg458Gly
XM_011513461.1:c.1306C>G	XP_011511763.1:p.Arg436Gly
XM_011513461.2:c.1306C>G	XP_011511763.1:p.Arg436Gly
XM_011513462.1:c.1225C>G	XP_011511764.1:p.Arg409Gly
XM_011513463.1:c.1225C>G	XP_011511765.1:p.Arg409Gly
XM_017008163.1:c.553C>G	XP_016863652.1:p.Arg185Gly
XR_924947.1:n.1582C>G