Canonical Allele Identifier: CA355963558

Gene: IDUA

Linked Data

• gnomAD v4: 4-1002750-C-A
• MyVariant Identifiers: chr4:g.996538C>A (hg19) ; chr4:g.1002750C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002750C>A , CM000666.2:g.1002750C>A	GRCh38
NC_000004.11:g.996538C>A , CM000666.1:g.996538C>A	GRCh37
NC_000004.10:g.986538C>A	NCBI36
NG_008103.1:g.20754C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1208C>A	ENSP00000247933.4:p.Ala403Asp
ENST00000514224.2:c.1208C>A MANE Select	ENSP00000425081.2:p.Ala403Asp
ENST00000652070.1:n.1264C>A
ENST00000247933.8:c.1208C>A	ENSP00000247933.4:p.Ala403Asp
ENST00000502829.1:n.10C>A
ENST00000514224.1:c.812C>A	ENSP00000425081.1:p.Ala271Asp
ENST00000514698.5:n.1315C>A
NM_000203.4:c.1208C>A	NP_000194.2:p.Ala403Asp
NR_110313.1:n.1296C>A
XM_006713882.2:c.812C>A	XP_006713945.1:p.Ala271Asp
XM_011513459.1:c.1274C>A	XP_011511761.1:p.Ala425Asp
XM_011513460.1:c.1067C>A	XP_011511762.1:p.Ala356Asp
XM_011513461.1:c.1001C>A	XP_011511763.1:p.Ala334Asp
XM_011513462.1:c.920C>A	XP_011511764.1:p.Ala307Asp
XM_011513463.1:c.920C>A	XP_011511765.1:p.Ala307Asp
XR_924947.1:n.1277C>A
NM_000203.5:c.1208C>A MANE Select	NP_000194.2:p.Ala403Asp
NM_001363576.1:c.812C>A	NP_001350505.1:p.Ala271Asp
XM_011513461.2:c.1001C>A	XP_011511763.1:p.Ala334Asp
XM_017008163.1:c.248C>A	XP_016863652.1:p.Ala83Asp