Canonical Allele Identifier: CA438058044

Gene: IDUA

Linked Data

• ClinVar Variation Id: 1123664
• ClinVar RCV Id: RCV001454801
• dbSNP Id: rs749848297
• MyVariant Identifiers: chr4:g.997378G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003590G>C , CM000666.2:g.1003590G>C	GRCh38
NC_000004.11:g.997378G>C , CM000666.1:g.997378G>C	GRCh37
NC_000004.10:g.987378G>C	NCBI36
NG_008103.1:g.21594G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1692G>C	ENSP00000247933.4:p.Leu564=
ENST00000514224.2:c.1692G>C MANE Select	ENSP00000425081.2:p.Leu564=
ENST00000652070.1:n.1748G>C
ENST00000247933.8:c.1692G>C	ENSP00000247933.4:p.Leu564=
ENST00000514224.1:c.1296G>C	ENSP00000425081.1:p.Leu432=
ENST00000514417.1:n.84G>C
ENST00000514698.5:n.1799G>C
NM_000203.4:c.1692G>C	NP_000194.2:p.Leu564=
NR_110313.1:n.1780G>C
XM_006713882.2:c.1296G>C	XP_006713945.1:p.Leu432=
XM_011513459.1:c.1758G>C	XP_011511761.1:p.Leu586=
XM_011513460.1:c.1551G>C	XP_011511762.1:p.Leu517=
XM_011513461.1:c.1485G>C	XP_011511763.1:p.Leu495=
XM_011513462.1:c.1404G>C	XP_011511764.1:p.Leu468=
XM_011513463.1:c.1404G>C	XP_011511765.1:p.Leu468=
XR_924947.1:n.1948G>C
NM_000203.5:c.1692G>C MANE Select	NP_000194.2:p.Leu564=
NM_001363576.1:c.1296G>C	NP_001350505.1:p.Leu432=
XM_011513461.2:c.1485G>C	XP_011511763.1:p.Leu495=
XM_017008163.1:c.732G>C	XP_016863652.1:p.Leu244=