Canonical Allele Identifier: CA1433071891

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003465G= , CM000666.2:g.1003465G=	GRCh38
NC_000004.11:g.997253G= , CM000666.1:g.997253G=	GRCh37
NC_000004.10:g.987253G=	NCBI36
NG_008103.1:g.21469G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1645G=	ENSP00000247933.4:p.Gly549=
ENST00000514224.2:c.1645G= MANE Select	ENSP00000425081.2:p.Gly549=
ENST00000652070.1:n.1701G=
ENST00000247933.8:c.1645G=	ENSP00000247933.4:p.Gly549=
ENST00000514224.1:c.1249G=	ENSP00000425081.1:p.Gly417=
ENST00000514417.1:n.37G=
ENST00000514698.5:n.1752G=
NM_000203.4:c.1645G=	NP_000194.2:p.Gly549=
NR_110313.1:n.1733G=
XM_006713882.2:c.1249G=	XP_006713945.1:p.Gly417=
XM_011513459.1:c.1711G=	XP_011511761.1:p.Gly571=
XM_011513460.1:c.1504G=	XP_011511762.1:p.Gly502=
XM_011513461.1:c.1438G=	XP_011511763.1:p.Gly480=
XM_011513462.1:c.1357G=	XP_011511764.1:p.Gly453=
XM_011513463.1:c.1357G=	XP_011511765.1:p.Gly453=
XR_924947.1:n.1901G=
NM_000203.5:c.1645G= MANE Select	NP_000194.2:p.Gly549=
NM_001363576.1:c.1249G=	NP_001350505.1:p.Gly417=
XM_011513461.2:c.1438G=	XP_011511763.1:p.Gly480=
XM_017008163.1:c.685G=	XP_016863652.1:p.Gly229=