Canonical Allele Identifier: CA355963893

Gene: IDUA

Linked Data

• gnomAD v4: 4-1002846-G-C
• MyVariant Identifiers: chr4:g.996634G>C (hg19) ; chr4:g.1002846G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002846G>C , CM000666.2:g.1002846G>C	GRCh38
NC_000004.11:g.996634G>C , CM000666.1:g.996634G>C	GRCh37
NC_000004.10:g.986634G>C	NCBI36
NG_008103.1:g.20850G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1304G>C	ENSP00000247933.4:p.Arg435Pro
ENST00000514224.2:c.1304G>C MANE Select	ENSP00000425081.2:p.Arg435Pro
ENST00000652070.1:n.1360G>C
ENST00000247933.8:c.1304G>C	ENSP00000247933.4:p.Arg435Pro
ENST00000502829.1:n.106G>C
ENST00000514224.1:c.908G>C	ENSP00000425081.1:p.Arg303Pro
ENST00000514698.5:n.1411G>C
NM_000203.4:c.1304G>C	NP_000194.2:p.Arg435Pro
NR_110313.1:n.1392G>C
XM_006713882.2:c.908G>C	XP_006713945.1:p.Arg303Pro
XM_011513459.1:c.1370G>C	XP_011511761.1:p.Arg457Pro
XM_011513460.1:c.1163G>C	XP_011511762.1:p.Arg388Pro
XM_011513461.1:c.1097G>C	XP_011511763.1:p.Arg366Pro
XM_011513462.1:c.1016G>C	XP_011511764.1:p.Arg339Pro
XM_011513463.1:c.1016G>C	XP_011511765.1:p.Arg339Pro
XR_924947.1:n.1373G>C
NM_000203.5:c.1304G>C MANE Select	NP_000194.2:p.Arg435Pro
NM_001363576.1:c.908G>C	NP_001350505.1:p.Arg303Pro
XM_011513461.2:c.1097G>C	XP_011511763.1:p.Arg366Pro
XM_017008163.1:c.344G>C	XP_016863652.1:p.Arg115Pro