Canonical Allele Identifier: CA1433071854

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003442G= , CM000666.2:g.1003442G=	GRCh38
NC_000004.11:g.997230G= , CM000666.1:g.997230G=	GRCh37
NC_000004.10:g.987230G=	NCBI36
NG_008103.1:g.21446G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1622G=	ENSP00000247933.4:p.Cys541=
ENST00000514224.2:c.1622G= MANE Select	ENSP00000425081.2:p.Cys541=
ENST00000652070.1:n.1678G=
ENST00000247933.8:c.1622G=	ENSP00000247933.4:p.Cys541=
ENST00000514224.1:c.1226G=	ENSP00000425081.1:p.Cys409=
ENST00000514417.1:n.14G=
ENST00000514698.5:n.1729G=
NM_000203.4:c.1622G=	NP_000194.2:p.Cys541=
NR_110313.1:n.1710G=
XM_006713882.2:c.1226G=	XP_006713945.1:p.Cys409=
XM_011513459.1:c.1688G=	XP_011511761.1:p.Cys563=
XM_011513460.1:c.1481G=	XP_011511762.1:p.Cys494=
XM_011513461.1:c.1415G=	XP_011511763.1:p.Cys472=
XM_011513462.1:c.1334G=	XP_011511764.1:p.Cys445=
XM_011513463.1:c.1334G=	XP_011511765.1:p.Cys445=
XR_924947.1:n.1878G=
NM_000203.5:c.1622G= MANE Select	NP_000194.2:p.Cys541=
NM_001363576.1:c.1226G=	NP_001350505.1:p.Cys409=
XM_011513461.2:c.1415G=	XP_011511763.1:p.Cys472=
XM_017008163.1:c.662G=	XP_016863652.1:p.Cys221=