Canonical Allele Identifier: CA355965170

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.997349C>T (hg19) ; chr4:g.1003561C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003561C>T , CM000666.2:g.1003561C>T	GRCh38
NC_000004.11:g.997349C>T , CM000666.1:g.997349C>T	GRCh37
NC_000004.10:g.987349C>T	NCBI36
NG_008103.1:g.21565C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1663C>T	ENSP00000247933.4:p.Arg555Cys
ENST00000514224.2:c.1663C>T MANE Select	ENSP00000425081.2:p.Arg555Cys
ENST00000652070.1:n.1719C>T
ENST00000247933.8:c.1663C>T	ENSP00000247933.4:p.Arg555Cys
ENST00000514224.1:c.1267C>T	ENSP00000425081.1:p.Arg423Cys
ENST00000514417.1:n.55C>T
ENST00000514698.5:n.1770C>T
NM_000203.4:c.1663C>T	NP_000194.2:p.Arg555Cys
NR_110313.1:n.1751C>T
XM_006713882.2:c.1267C>T	XP_006713945.1:p.Arg423Cys
XM_011513459.1:c.1729C>T	XP_011511761.1:p.Arg577Cys
XM_011513460.1:c.1522C>T	XP_011511762.1:p.Arg508Cys
XM_011513461.1:c.1456C>T	XP_011511763.1:p.Arg486Cys
XM_011513462.1:c.1375C>T	XP_011511764.1:p.Arg459Cys
XM_011513463.1:c.1375C>T	XP_011511765.1:p.Arg459Cys
XR_924947.1:n.1919C>T
NM_000203.5:c.1663C>T MANE Select	NP_000194.2:p.Arg555Cys
NM_001363576.1:c.1267C>T	NP_001350505.1:p.Arg423Cys
XM_011513461.2:c.1456C>T	XP_011511763.1:p.Arg486Cys
XM_017008163.1:c.703C>T	XP_016863652.1:p.Arg235Cys