Canonical Allele Identifier: CA1433071848

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003439T= , CM000666.2:g.1003439T=	GRCh38
NC_000004.11:g.997227T= , CM000666.1:g.997227T=	GRCh37
NC_000004.10:g.987227T=	NCBI36
NG_008103.1:g.21443T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1619T=	ENSP00000247933.4:p.Val540=
ENST00000514224.2:c.1619T= MANE Select	ENSP00000425081.2:p.Val540=
ENST00000652070.1:n.1675T=
ENST00000247933.8:c.1619T=	ENSP00000247933.4:p.Val540=
ENST00000514224.1:c.1223T=	ENSP00000425081.1:p.Val408=
ENST00000514417.1:n.11T=
ENST00000514698.5:n.1726T=
NM_000203.4:c.1619T=	NP_000194.2:p.Val540=
NR_110313.1:n.1707T=
XM_006713882.2:c.1223T=	XP_006713945.1:p.Val408=
XM_011513459.1:c.1685T=	XP_011511761.1:p.Val562=
XM_011513460.1:c.1478T=	XP_011511762.1:p.Val493=
XM_011513461.1:c.1412T=	XP_011511763.1:p.Val471=
XM_011513462.1:c.1331T=	XP_011511764.1:p.Val444=
XM_011513463.1:c.1331T=	XP_011511765.1:p.Val444=
XR_924947.1:n.1875T=
NM_000203.5:c.1619T= MANE Select	NP_000194.2:p.Val540=
NM_001363576.1:c.1223T=	NP_001350505.1:p.Val408=
XM_011513461.2:c.1412T=	XP_011511763.1:p.Val471=
XM_017008163.1:c.659T=	XP_016863652.1:p.Val220=