Canonical Allele Identifier: CA2802130

Gene: IDUA

Linked Data

• dbSNP Id: rs370267649
• ExAC: 4:995953 G / A
• gnomAD v2: 4-995953-G-A
• gnomAD v4: 4-1002165-G-A
• MyVariant Identifiers: chr4:g.995953G>A (hg19) ; chr4:g.1002165G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002165G>A , CM000666.2:g.1002165G>A	GRCh38
NC_000004.11:g.995953G>A , CM000666.1:g.995953G>A	GRCh37
NC_000004.10:g.985953G>A	NCBI36
NG_008103.1:g.20169G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.972+4G>A	ENSP00000247933.4:n.972+4G>A
ENST00000514224.2:c.972+4G>A MANE Select	ENSP00000425081.2:n.972+4G>A
ENST00000652070.1:n.1028+4G>A
ENST00000247933.8:c.972+4G>A	ENSP00000247933.4:n.972+4G>A
ENST00000514224.1:c.576+4G>A	ENSP00000425081.1:n.576+4G>A
ENST00000514698.5:n.976G>A
NM_000203.4:c.972+4G>A	NP_000194.2:n.972+4G>A
NR_110313.1:n.1060+4G>A
XM_006713882.2:c.576+4G>A	XP_006713945.1:n.576+4G>A
XM_011513459.1:c.935G>A	XP_011511761.1:p.Gly312Glu
XM_011513460.1:c.831+4G>A	XP_011511762.1:n.831+4G>A
XM_011513461.1:c.765+4G>A	XP_011511763.1:n.765+4G>A
XM_011513462.1:c.684+4G>A	XP_011511764.1:n.684+4G>A
XM_011513463.1:c.684+4G>A	XP_011511765.1:n.684+4G>A
XR_924947.1:n.1041+4G>A
NM_000203.5:c.972+4G>A MANE Select	NP_000194.2:n.972+4G>A
NM_001363576.1:c.576+4G>A	NP_001350505.1:n.576+4G>A
XM_011513461.2:c.765+4G>A	XP_011511763.1:n.765+4G>A
XM_017008163.1:c.12+4G>A	XP_016863652.1:n.12+4G>A