Canonical Allele Identifier: CA1433072259

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003619G= , CM000666.2:g.1003619G=	GRCh38
NC_000004.11:g.997407G= , CM000666.1:g.997407G=	GRCh37
NC_000004.10:g.987407G=	NCBI36
NG_008103.1:g.21623G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1721G=	ENSP00000247933.4:p.Gly574=
ENST00000514224.2:c.1721G= MANE Select	ENSP00000425081.2:p.Gly574=
ENST00000652070.1:n.1777G=
ENST00000247933.8:c.1721G=	ENSP00000247933.4:p.Gly574=
ENST00000514224.1:c.1325G=	ENSP00000425081.1:p.Gly442=
ENST00000514417.1:n.113G=
ENST00000514698.5:n.1828G=
NM_000203.4:c.1721G=	NP_000194.2:p.Gly574=
NR_110313.1:n.1809G=
XM_006713882.2:c.1325G=	XP_006713945.1:p.Gly442=
XM_011513459.1:c.1787G=	XP_011511761.1:p.Gly596=
XM_011513460.1:c.1580G=	XP_011511762.1:p.Gly527=
XM_011513461.1:c.1514G=	XP_011511763.1:p.Gly505=
XM_011513462.1:c.1433G=	XP_011511764.1:p.Gly478=
XM_011513463.1:c.1433G=	XP_011511765.1:p.Gly478=
XR_924947.1:n.1977G=
NM_000203.5:c.1721G= MANE Select	NP_000194.2:p.Gly574=
NM_001363576.1:c.1325G=	NP_001350505.1:p.Gly442=
XM_011513461.2:c.1514G=	XP_011511763.1:p.Gly505=
XM_017008163.1:c.761G=	XP_016863652.1:p.Gly254=