Canonical Allele Identifier: CA2739858837

Gene: IDUA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001912T>A , CM000666.2:g.1001912T>A	GRCh38
NC_000004.11:g.995700T>A , CM000666.1:g.995700T>A	GRCh37
NC_000004.10:g.985700T>A	NCBI36
NG_008103.1:g.19916T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.792+31T>A	ENSP00000247933.4:n.792+31T>A
ENST00000514224.2:c.792+31T>A MANE Select	ENSP00000425081.2:n.792+31T>A
ENST00000652070.1:n.848+31T>A
ENST00000247933.8:c.792+31T>A	ENSP00000247933.4:n.792+31T>A
ENST00000502910.5:c.651+31T>A	ENSP00000422952.1:n.651+31T>A
ENST00000514192.5:c.609+31T>A	ENSP00000423685.1:n.609+31T>A
ENST00000514224.1:c.396+31T>A	ENSP00000425081.1:n.396+31T>A
ENST00000514698.5:n.723T>A
NM_000203.4:c.792+31T>A	NP_000194.2:n.792+31T>A
NR_110313.1:n.880+31T>A
XM_006713882.2:c.396+31T>A	XP_006713945.1:n.396+31T>A
XM_011513459.1:c.682T>A	XP_011511761.1:p.Phe228Ile
XM_011513460.1:c.651+31T>A	XP_011511762.1:n.651+31T>A
XM_011513461.1:c.585+31T>A	XP_011511763.1:n.585+31T>A
XM_011513462.1:c.504+31T>A	XP_011511764.1:n.504+31T>A
XM_011513463.1:c.504+31T>A	XP_011511765.1:n.504+31T>A
XR_924947.1:n.861+31T>A
NM_000203.5:c.792+31T>A MANE Select	NP_000194.2:n.792+31T>A
NM_001363576.1:c.396+31T>A	NP_001350505.1:n.396+31T>A
XM_011513461.2:c.585+31T>A	XP_011511763.1:n.585+31T>A
XM_017008163.1:c.-169+31T>A	XP_016863652.1:n.-169+31T>A