Canonical Allele Identifier: CA1433071346

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003138G= , CM000666.2:g.1003138G=	GRCh38
NC_000004.11:g.996926G= , CM000666.1:g.996926G=	GRCh37
NC_000004.10:g.986926G=	NCBI36
NG_008103.1:g.21142G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1505G=	ENSP00000247933.4:p.Arg502=
ENST00000514224.2:c.1505G= MANE Select	ENSP00000425081.2:p.Arg502=
ENST00000652070.1:n.1561G=
ENST00000247933.8:c.1505G=	ENSP00000247933.4:p.Arg502=
ENST00000502829.1:n.307G=
ENST00000514224.1:c.1109G=	ENSP00000425081.1:p.Arg370=
ENST00000514698.5:n.1612G=
NM_000203.4:c.1505G=	NP_000194.2:p.Arg502=
NR_110313.1:n.1593G=
XM_006713882.2:c.1109G=	XP_006713945.1:p.Arg370=
XM_011513459.1:c.1571G=	XP_011511761.1:p.Arg524=
XM_011513460.1:c.1364G=	XP_011511762.1:p.Arg455=
XM_011513461.1:c.1298G=	XP_011511763.1:p.Arg433=
XM_011513462.1:c.1217G=	XP_011511764.1:p.Arg406=
XM_011513463.1:c.1217G=	XP_011511765.1:p.Arg406=
XR_924947.1:n.1574G=
NM_000203.5:c.1505G= MANE Select	NP_000194.2:p.Arg502=
NM_001363576.1:c.1109G=	NP_001350505.1:p.Arg370=
XM_011513461.2:c.1298G=	XP_011511763.1:p.Arg433=
XM_017008163.1:c.545G=	XP_016863652.1:p.Arg182=