Canonical Allele Identifier: CA1433068450

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002001C= , CM000666.2:g.1002001C=	GRCh38
NC_000004.11:g.995789C= , CM000666.1:g.995789C=	GRCh37
NC_000004.10:g.985789C=	NCBI36
NG_008103.1:g.20005C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.812C=	ENSP00000247933.4:p.Ser271=
ENST00000514224.2:c.812C= MANE Select	ENSP00000425081.2:p.Ser271=
ENST00000652070.1:n.868C=
ENST00000247933.8:c.812C=	ENSP00000247933.4:p.Ser271=
ENST00000502910.5:c.671C=	ENSP00000422952.1:p.Ser224=
ENST00000514192.5:c.629C=	ENSP00000423685.1:p.Ser210=
ENST00000514224.1:c.416C=	ENSP00000425081.1:p.Ser139=
ENST00000514698.5:n.812C=
NM_000203.4:c.812C=	NP_000194.2:p.Ser271=
NR_110313.1:n.900C=
XM_006713882.2:c.416C=	XP_006713945.1:p.Ser139=
XM_011513459.1:c.771C=	XP_011511761.1:p.Leu257=
XM_011513460.1:c.671C=	XP_011511762.1:p.Ser224=
XM_011513461.1:c.605C=	XP_011511763.1:p.Ser202=
XM_011513462.1:c.524C=	XP_011511764.1:p.Ser175=
XM_011513463.1:c.524C=	XP_011511765.1:p.Ser175=
XR_924947.1:n.881C=
NM_000203.5:c.812C= MANE Select	NP_000194.2:p.Ser271=
NM_001363576.1:c.416C=	NP_001350505.1:p.Ser139=
XM_011513461.2:c.605C=	XP_011511763.1:p.Ser202=
XM_017008163.1:c.-149C=	XP_016863652.1:n.-149C=