Canonical Allele Identifier: CA438058003

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.997345G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003557G>T , CM000666.2:g.1003557G>T	GRCh38
NC_000004.11:g.997345G>T , CM000666.1:g.997345G>T	GRCh37
NC_000004.10:g.987345G>T	NCBI36
NG_008103.1:g.21561G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1659G>T	ENSP00000247933.4:p.Arg553=
ENST00000514224.2:c.1659G>T MANE Select	ENSP00000425081.2:p.Arg553=
ENST00000652070.1:n.1715G>T
ENST00000247933.8:c.1659G>T	ENSP00000247933.4:p.Arg553=
ENST00000514224.1:c.1263G>T	ENSP00000425081.1:p.Arg421=
ENST00000514417.1:n.51G>T
ENST00000514698.5:n.1766G>T
NM_000203.4:c.1659G>T	NP_000194.2:p.Arg553=
NR_110313.1:n.1747G>T
XM_006713882.2:c.1263G>T	XP_006713945.1:p.Arg421=
XM_011513459.1:c.1725G>T	XP_011511761.1:p.Arg575=
XM_011513460.1:c.1518G>T	XP_011511762.1:p.Arg506=
XM_011513461.1:c.1452G>T	XP_011511763.1:p.Arg484=
XM_011513462.1:c.1371G>T	XP_011511764.1:p.Arg457=
XM_011513463.1:c.1371G>T	XP_011511765.1:p.Arg457=
XR_924947.1:n.1915G>T
NM_000203.5:c.1659G>T MANE Select	NP_000194.2:p.Arg553=
NM_001363576.1:c.1263G>T	NP_001350505.1:p.Arg421=
XM_011513461.2:c.1452G>T	XP_011511763.1:p.Arg484=
XM_017008163.1:c.699G>T	XP_016863652.1:p.Arg233=