Canonical Allele Identifier: CA1433071334

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003134T= , CM000666.2:g.1003134T=	GRCh38
NC_000004.11:g.996922T= , CM000666.1:g.996922T=	GRCh37
NC_000004.10:g.986922T=	NCBI36
NG_008103.1:g.21138T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1501T=	ENSP00000247933.4:p.Phe501=
ENST00000514224.2:c.1501T= MANE Select	ENSP00000425081.2:p.Phe501=
ENST00000652070.1:n.1557T=
ENST00000247933.8:c.1501T=	ENSP00000247933.4:p.Phe501=
ENST00000502829.1:n.303T=
ENST00000514224.1:c.1105T=	ENSP00000425081.1:p.Phe369=
ENST00000514698.5:n.1608T=
NM_000203.4:c.1501T=	NP_000194.2:p.Phe501=
NR_110313.1:n.1589T=
XM_006713882.2:c.1105T=	XP_006713945.1:p.Phe369=
XM_011513459.1:c.1567T=	XP_011511761.1:p.Phe523=
XM_011513460.1:c.1360T=	XP_011511762.1:p.Phe454=
XM_011513461.1:c.1294T=	XP_011511763.1:p.Phe432=
XM_011513462.1:c.1213T=	XP_011511764.1:p.Phe405=
XM_011513463.1:c.1213T=	XP_011511765.1:p.Phe405=
XR_924947.1:n.1570T=
NM_000203.5:c.1501T= MANE Select	NP_000194.2:p.Phe501=
NM_001363576.1:c.1105T=	NP_001350505.1:p.Phe369=
XM_011513461.2:c.1294T=	XP_011511763.1:p.Phe432=
XM_017008163.1:c.541T=	XP_016863652.1:p.Phe181=