Canonical Allele Identifier: CA1433069056

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002299G= , CM000666.2:g.1002299G=	GRCh38
NC_000004.11:g.996087G= , CM000666.1:g.996087G=	GRCh37
NC_000004.10:g.986087G=	NCBI36
NG_008103.1:g.20303G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1003G=	ENSP00000247933.4:p.Ala335=
ENST00000514224.2:c.1003G= MANE Select	ENSP00000425081.2:p.Ala335=
ENST00000652070.1:n.1059G=
ENST00000247933.8:c.1003G=	ENSP00000247933.4:p.Ala335=
ENST00000514224.1:c.607G=	ENSP00000425081.1:p.Ala203=
ENST00000514698.5:n.1110G=
NM_000203.4:c.1003G=	NP_000194.2:p.Ala335=
NR_110313.1:n.1091G=
XM_006713882.2:c.607G=	XP_006713945.1:p.Ala203=
XM_011513459.1:c.1069G=	XP_011511761.1:p.Ala357=
XM_011513460.1:c.862G=	XP_011511762.1:p.Ala288=
XM_011513461.1:c.796G=	XP_011511763.1:p.Ala266=
XM_011513462.1:c.715G=	XP_011511764.1:p.Ala239=
XM_011513463.1:c.715G=	XP_011511765.1:p.Ala239=
XR_924947.1:n.1072G=
NM_000203.5:c.1003G= MANE Select	NP_000194.2:p.Ala335=
NM_001363576.1:c.607G=	NP_001350505.1:p.Ala203=
XM_011513461.2:c.796G=	XP_011511763.1:p.Ala266=
XM_017008163.1:c.43G=	XP_016863652.1:p.Ala15=