Canonical Allele Identifier: CA1433071824

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003418C= , CM000666.2:g.1003418C=	GRCh38
NC_000004.11:g.997206C= , CM000666.1:g.997206C=	GRCh37
NC_000004.10:g.987206C=	NCBI36
NG_008103.1:g.21422C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000203.5:c.1598C= MANE Select	NP_000194.2:p.Pro533=
ENST00000514224.2:c.1598C= MANE Select	ENSP00000425081.2:p.Pro533=
NM_000203.4:c.1598C=	NP_000194.2:p.Pro533=
NM_001363576.1:c.1202C=	NP_001350505.1:p.Pro401=
NR_110313.1:n.1686C=
ENST00000247933.8:c.1598C=	ENSP00000247933.4:p.Pro533=
ENST00000247933.9:c.1598C=	ENSP00000247933.4:p.Pro533=
ENST00000514224.1:c.1202C=	ENSP00000425081.1:p.Pro401=
ENST00000514698.5:n.1705C=
ENST00000652070.1:n.1654C=
XM_006713882.2:c.1202C=	XP_006713945.1:p.Pro401=
XM_011513459.1:c.1664C=	XP_011511761.1:p.Pro555=
XM_011513460.1:c.1457C=	XP_011511762.1:p.Pro486=
XM_011513461.1:c.1391C=	XP_011511763.1:p.Pro464=
XM_011513461.2:c.1391C=	XP_011511763.1:p.Pro464=
XM_011513462.1:c.1310C=	XP_011511764.1:p.Pro437=
XM_011513463.1:c.1310C=	XP_011511765.1:p.Pro437=
XM_017008163.1:c.638C=	XP_016863652.1:p.Pro213=
XR_924947.1:n.1854C=