Canonical Allele Identifier: CA355965033

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.997209C>A (hg19) ; chr4:g.1003421C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003421C>A , CM000666.2:g.1003421C>A	GRCh38
NC_000004.11:g.997209C>A , CM000666.1:g.997209C>A	GRCh37
NC_000004.10:g.987209C>A	NCBI36
NG_008103.1:g.21425C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000247933.9:c.1601C>A	ENSP00000247933.4:p.Ser534Ter
ENST00000514224.2:c.1601C>A MANE Select	ENSP00000425081.2:p.Ser534Ter
ENST00000652070.1:n.1657C>A
ENST00000247933.8:c.1601C>A	ENSP00000247933.4:p.Ser534Ter
ENST00000514224.1:c.1205C>A	ENSP00000425081.1:p.Ser402Ter
ENST00000514698.5:n.1708C>A
NM_000203.4:c.1601C>A	NP_000194.2:p.Ser534Ter
NR_110313.1:n.1689C>A
XM_006713882.2:c.1205C>A	XP_006713945.1:p.Ser402Ter
XM_011513459.1:c.1667C>A	XP_011511761.1:p.Ser556Ter
XM_011513460.1:c.1460C>A	XP_011511762.1:p.Ser487Ter
XM_011513461.1:c.1394C>A	XP_011511763.1:p.Ser465Ter
XM_011513462.1:c.1313C>A	XP_011511764.1:p.Ser438Ter
XM_011513463.1:c.1313C>A	XP_011511765.1:p.Ser438Ter
XR_924947.1:n.1857C>A
NM_000203.5:c.1601C>A MANE Select	NP_000194.2:p.Ser534Ter
NM_001363576.1:c.1205C>A	NP_001350505.1:p.Ser402Ter
XM_011513461.2:c.1394C>A	XP_011511763.1:p.Ser465Ter
XM_017008163.1:c.641C>A	XP_016863652.1:p.Ser214Ter