Canonical Allele Identifier: CA1433071196

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003102T= , CM000666.2:g.1003102T=	GRCh38
NC_000004.11:g.996890T= , CM000666.1:g.996890T=	GRCh37
NC_000004.10:g.986890T=	NCBI36
NG_008103.1:g.21106T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000203.5:c.1469T= MANE Select	NP_000194.2:p.Leu490=
ENST00000514224.2:c.1469T= MANE Select	ENSP00000425081.2:p.Leu490=
NM_000203.4:c.1469T=	NP_000194.2:p.Leu490=
NM_001363576.1:c.1073T=	NP_001350505.1:p.Leu358=
NR_110313.1:n.1557T=
ENST00000247933.8:c.1469T=	ENSP00000247933.4:p.Leu490=
ENST00000247933.9:c.1469T=	ENSP00000247933.4:p.Leu490=
ENST00000502829.1:n.271T=
ENST00000514224.1:c.1073T=	ENSP00000425081.1:p.Leu358=
ENST00000514698.5:n.1576T=
ENST00000652070.1:n.1525T=
XM_006713882.2:c.1073T=	XP_006713945.1:p.Leu358=
XM_011513459.1:c.1535T=	XP_011511761.1:p.Leu512=
XM_011513460.1:c.1328T=	XP_011511762.1:p.Leu443=
XM_011513461.1:c.1262T=	XP_011511763.1:p.Leu421=
XM_011513461.2:c.1262T=	XP_011511763.1:p.Leu421=
XM_011513462.1:c.1181T=	XP_011511764.1:p.Leu394=
XM_011513463.1:c.1181T=	XP_011511765.1:p.Leu394=
XM_017008163.1:c.509T=	XP_016863652.1:p.Leu170=
XR_924947.1:n.1538T=