Canonical Allele Identifier: CA1433068148

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001866C= , CM000666.2:g.1001866C=	GRCh38
NC_000004.11:g.995654C= , CM000666.1:g.995654C=	GRCh37
NC_000004.10:g.985654C=	NCBI36
NG_008103.1:g.19870C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.777C=	ENSP00000247933.4:p.Ile259=
ENST00000514224.2:c.777C= MANE Select	ENSP00000425081.2:p.Ile259=
ENST00000652070.1:n.833C=
ENST00000247933.8:c.777C=	ENSP00000247933.4:p.Ile259=
ENST00000502910.5:c.636C=	ENSP00000422952.1:p.Ile212=
ENST00000514192.5:c.594C=	ENSP00000423685.1:p.Ile198=
ENST00000514224.1:c.381C=	ENSP00000425081.1:p.Ile127=
ENST00000514698.5:n.677C=
NM_000203.4:c.777C=	NP_000194.2:p.Ile259=
NR_110313.1:n.865C=
XM_006713882.2:c.381C=	XP_006713945.1:p.Ile127=
XM_011513459.1:c.636C=	XP_011511761.1:p.Ile212=
XM_011513460.1:c.636C=	XP_011511762.1:p.Ile212=
XM_011513461.1:c.570C=	XP_011511763.1:p.Ile190=
XM_011513462.1:c.489C=	XP_011511764.1:p.Ile163=
XM_011513463.1:c.489C=	XP_011511765.1:p.Ile163=
XR_924947.1:n.846C=
NM_000203.5:c.777C= MANE Select	NP_000194.2:p.Ile259=
NM_001363576.1:c.381C=	NP_001350505.1:p.Ile127=
XM_011513461.2:c.570C=	XP_011511763.1:p.Ile190=
XM_017008163.1:c.-184C=	XP_016863652.1:n.-184C=