Canonical Allele Identifier: CA1433071786

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003364C= , CM000666.2:g.1003364C=	GRCh38
NC_000004.11:g.997152C= , CM000666.1:g.997152C=	GRCh37
NC_000004.10:g.987152C=	NCBI36
NG_008103.1:g.21368C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1544C=	ENSP00000247933.4:p.Pro515=
ENST00000514224.2:c.1544C= MANE Select	ENSP00000425081.2:p.Pro515=
ENST00000652070.1:n.1600C=
ENST00000247933.8:c.1544C=	ENSP00000247933.4:p.Pro515=
ENST00000502829.1:n.533C=
ENST00000514224.1:c.1148C=	ENSP00000425081.1:p.Pro383=
ENST00000514698.5:n.1651C=
NM_000203.4:c.1544C=	NP_000194.2:p.Pro515=
NR_110313.1:n.1632C=
XM_006713882.2:c.1148C=	XP_006713945.1:p.Pro383=
XM_011513459.1:c.1610C=	XP_011511761.1:p.Pro537=
XM_011513460.1:c.1403C=	XP_011511762.1:p.Pro468=
XM_011513461.1:c.1337C=	XP_011511763.1:p.Pro446=
XM_011513462.1:c.1256C=	XP_011511764.1:p.Pro419=
XM_011513463.1:c.1256C=	XP_011511765.1:p.Pro419=
XR_924947.1:n.1800C=
NM_000203.5:c.1544C= MANE Select	NP_000194.2:p.Pro515=
NM_001363576.1:c.1148C=	NP_001350505.1:p.Pro383=
XM_011513461.2:c.1337C=	XP_011511763.1:p.Pro446=
XM_017008163.1:c.584C=	XP_016863652.1:p.Pro195=