Canonical Allele Identifier: CA355962266

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.995665G>C (hg19) ; chr4:g.1001877G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001877G>C , CM000666.2:g.1001877G>C	GRCh38
NC_000004.11:g.995665G>C , CM000666.1:g.995665G>C	GRCh37
NC_000004.10:g.985665G>C	NCBI36
NG_008103.1:g.19881G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.788G>C	ENSP00000247933.4:p.Arg263Thr
ENST00000514224.2:c.788G>C MANE Select	ENSP00000425081.2:p.Arg263Thr
ENST00000652070.1:n.844G>C
ENST00000247933.8:c.788G>C	ENSP00000247933.4:p.Arg263Thr
ENST00000502910.5:c.647G>C	ENSP00000422952.1:p.Arg216Thr
ENST00000514192.5:c.605G>C	ENSP00000423685.1:p.Arg202Thr
ENST00000514224.1:c.392G>C	ENSP00000425081.1:p.Arg131Thr
ENST00000514698.5:n.688G>C
NM_000203.4:c.788G>C	NP_000194.2:p.Arg263Thr
NR_110313.1:n.876G>C
XM_006713882.2:c.392G>C	XP_006713945.1:p.Arg131Thr
XM_011513459.1:c.647G>C	XP_011511761.1:p.Arg216Thr
XM_011513460.1:c.647G>C	XP_011511762.1:p.Arg216Thr
XM_011513461.1:c.581G>C	XP_011511763.1:p.Arg194Thr
XM_011513462.1:c.500G>C	XP_011511764.1:p.Arg167Thr
XM_011513463.1:c.500G>C	XP_011511765.1:p.Arg167Thr
XR_924947.1:n.857G>C
NM_000203.5:c.788G>C MANE Select	NP_000194.2:p.Arg263Thr
NM_001363576.1:c.392G>C	NP_001350505.1:p.Arg131Thr
XM_011513461.2:c.581G>C	XP_011511763.1:p.Arg194Thr
XM_017008163.1:c.-173G>C	XP_016863652.1:n.-173G>C