Canonical Allele Identifier: CA2669480178

Gene: IDUA

Linked Data

• gnomAD v4: 4-1001931-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001931G>A , CM000666.2:g.1001931G>A	GRCh38
NC_000004.11:g.995719G>A , CM000666.1:g.995719G>A	GRCh37
NC_000004.10:g.985719G>A	NCBI36
NG_008103.1:g.19935G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.793-51G>A	ENSP00000247933.4:n.793-51G>A
ENST00000514224.2:c.793-51G>A MANE Select	ENSP00000425081.2:n.793-51G>A
ENST00000652070.1:n.849-51G>A
ENST00000247933.8:c.793-51G>A	ENSP00000247933.4:n.793-51G>A
ENST00000502910.5:c.652-51G>A	ENSP00000422952.1:n.652-51G>A
ENST00000514192.5:c.610-51G>A	ENSP00000423685.1:n.610-51G>A
ENST00000514224.1:c.397-51G>A	ENSP00000425081.1:n.397-51G>A
ENST00000514698.5:n.742G>A
NM_000203.4:c.793-51G>A	NP_000194.2:n.793-51G>A
NR_110313.1:n.881-51G>A
XM_006713882.2:c.397-51G>A	XP_006713945.1:n.397-51G>A
XM_011513459.1:c.701G>A	XP_011511761.1:p.Cys234Tyr
XM_011513460.1:c.652-51G>A	XP_011511762.1:n.652-51G>A
XM_011513461.1:c.586-51G>A	XP_011511763.1:n.586-51G>A
XM_011513462.1:c.505-51G>A	XP_011511764.1:n.505-51G>A
XM_011513463.1:c.505-51G>A	XP_011511765.1:n.505-51G>A
XR_924947.1:n.862-51G>A
NM_000203.5:c.793-51G>A MANE Select	NP_000194.2:n.793-51G>A
NM_001363576.1:c.397-51G>A	NP_001350505.1:n.397-51G>A
XM_011513461.2:c.586-51G>A	XP_011511763.1:n.586-51G>A
XM_017008163.1:c.-168-51G>A	XP_016863652.1:n.-168-51G>A