Canonical Allele Identifier: CA1433068815

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002162G= , CM000666.2:g.1002162G=	GRCh38
NC_000004.11:g.995950G= , CM000666.1:g.995950G=	GRCh37
NC_000004.10:g.985950G=	NCBI36
NG_008103.1:g.20166G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.972+1G=	ENSP00000247933.4:n.972+1G=
ENST00000514224.2:c.972+1G= MANE Select	ENSP00000425081.2:n.972+1G=
ENST00000652070.1:n.1028+1G=
ENST00000247933.8:c.972+1G=	ENSP00000247933.4:n.972+1G=
ENST00000514224.1:c.576+1G=	ENSP00000425081.1:n.576+1G=
ENST00000514698.5:n.973G=
NM_000203.4:c.972+1G=	NP_000194.2:n.972+1G=
NR_110313.1:n.1060+1G=
XM_006713882.2:c.576+1G=	XP_006713945.1:n.576+1G=
XM_011513459.1:c.932G=	XP_011511761.1:p.Gly311=
XM_011513460.1:c.831+1G=	XP_011511762.1:n.831+1G=
XM_011513461.1:c.765+1G=	XP_011511763.1:n.765+1G=
XM_011513462.1:c.684+1G=	XP_011511764.1:n.684+1G=
XM_011513463.1:c.684+1G=	XP_011511765.1:n.684+1G=
XR_924947.1:n.1041+1G=
NM_000203.5:c.972+1G= MANE Select	NP_000194.2:n.972+1G=
NM_001363576.1:c.576+1G=	NP_001350505.1:n.576+1G=
XM_011513461.2:c.765+1G=	XP_011511763.1:n.765+1G=
XM_017008163.1:c.12+1G=	XP_016863652.1:n.12+1G=