Canonical Allele Identifier: CA437918922

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001532C>T , CM000666.2:g.1001532C>T	GRCh38
NC_000004.11:g.995320C>T , CM000666.1:g.995320C>T	GRCh37
NC_000004.10:g.985320C>T	NCBI36
NG_008103.1:g.19536C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.558C>T	ENSP00000247933.4:p.His186=
ENST00000514224.2:c.558C>T MANE Select	ENSP00000425081.2:p.His186=
ENST00000652070.1:n.614C>T
ENST00000247933.8:c.558C>T	ENSP00000247933.4:p.His186=
ENST00000502910.5:c.417C>T	ENSP00000422952.1:p.His139=
ENST00000504568.5:c.518C>T
ENST00000509948.5:c.351C>T	ENSP00000424227.1:p.His117=
ENST00000514192.5:c.375C>T	ENSP00000423685.1:p.His125=
ENST00000514224.1:c.162C>T	ENSP00000425081.1:p.His54=
ENST00000514698.5:n.458C>T
NM_000203.4:c.558C>T	NP_000194.2:p.His186=
NR_110313.1:n.646C>T
XM_006713882.2:c.162C>T	XP_006713945.1:p.His54=
XM_011513459.1:c.417C>T	XP_011511761.1:p.His139=
XM_011513460.1:c.417C>T	XP_011511762.1:p.His139=
XM_011513461.1:c.351C>T	XP_011511763.1:p.His117=
XM_011513462.1:c.270C>T	XP_011511764.1:p.His90=
XM_011513463.1:c.270C>T	XP_011511765.1:p.His90=
XR_924947.1:n.627C>T
NM_000203.5:c.558C>T MANE Select	NP_000194.2:p.His186=
NM_001363576.1:c.162C>T	NP_001350505.1:p.His54=
XM_011513461.2:c.351C>T	XP_011511763.1:p.His117=
XM_017008163.1:c.-431C>T	XP_016863652.1:n.-431C>T