Canonical Allele Identifier: CA355961957

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.995506G>C (hg19) ; chr4:g.1001718G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001718G>C , CM000666.2:g.1001718G>C	GRCh38
NC_000004.11:g.995506G>C , CM000666.1:g.995506G>C	GRCh37
NC_000004.10:g.985506G>C	NCBI36
NG_008103.1:g.19722G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.629G>C	ENSP00000247933.4:p.Arg210Pro
ENST00000514224.2:c.629G>C MANE Select	ENSP00000425081.2:p.Arg210Pro
ENST00000652070.1:n.685G>C
ENST00000247933.8:c.629G>C	ENSP00000247933.4:p.Arg210Pro
ENST00000502910.5:c.488G>C	ENSP00000422952.1:p.Arg163Pro
ENST00000509948.5:c.422G>C	ENSP00000424227.1:p.Arg141Pro
ENST00000514192.5:c.446G>C	ENSP00000423685.1:p.Arg149Pro
ENST00000514224.1:c.233G>C	ENSP00000425081.1:p.Arg78Pro
ENST00000514698.5:n.529G>C
NM_000203.4:c.629G>C	NP_000194.2:p.Arg210Pro
NR_110313.1:n.717G>C
XM_006713882.2:c.233G>C	XP_006713945.1:p.Arg78Pro
XM_011513459.1:c.488G>C	XP_011511761.1:p.Arg163Pro
XM_011513460.1:c.488G>C	XP_011511762.1:p.Arg163Pro
XM_011513461.1:c.422G>C	XP_011511763.1:p.Arg141Pro
XM_011513462.1:c.341G>C	XP_011511764.1:p.Arg114Pro
XM_011513463.1:c.341G>C	XP_011511765.1:p.Arg114Pro
XR_924947.1:n.698G>C
NM_000203.5:c.629G>C MANE Select	NP_000194.2:p.Arg210Pro
NM_001363576.1:c.233G>C	NP_001350505.1:p.Arg78Pro
XM_011513461.2:c.422G>C	XP_011511763.1:p.Arg141Pro
XM_017008163.1:c.-332G>C	XP_016863652.1:n.-332G>C