Canonical Allele Identifier: CA355962294

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.995773G>C (hg19) ; chr4:g.1001985G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001985G>C , CM000666.2:g.1001985G>C	GRCh38
NC_000004.11:g.995773G>C , CM000666.1:g.995773G>C	GRCh37
NC_000004.10:g.985773G>C	NCBI36
NG_008103.1:g.19989G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.796G>C	ENSP00000247933.4:p.Ala266Pro
ENST00000514224.2:c.796G>C MANE Select	ENSP00000425081.2:p.Ala266Pro
ENST00000652070.1:n.852G>C
ENST00000247933.8:c.796G>C	ENSP00000247933.4:p.Ala266Pro
ENST00000502910.5:c.655G>C	ENSP00000422952.1:p.Ala219Pro
ENST00000514192.5:c.613G>C	ENSP00000423685.1:p.Ala205Pro
ENST00000514224.1:c.400G>C	ENSP00000425081.1:p.Ala134Pro
ENST00000514698.5:n.796G>C
NM_000203.4:c.796G>C	NP_000194.2:p.Ala266Pro
NR_110313.1:n.884G>C
XM_006713882.2:c.400G>C	XP_006713945.1:p.Ala134Pro
XM_011513459.1:c.755G>C	XP_011511761.1:p.Cys252Ser
XM_011513460.1:c.655G>C	XP_011511762.1:p.Ala219Pro
XM_011513461.1:c.589G>C	XP_011511763.1:p.Ala197Pro
XM_011513462.1:c.508G>C	XP_011511764.1:p.Ala170Pro
XM_011513463.1:c.508G>C	XP_011511765.1:p.Ala170Pro
XR_924947.1:n.865G>C
NM_000203.5:c.796G>C MANE Select	NP_000194.2:p.Ala266Pro
NM_001363576.1:c.400G>C	NP_001350505.1:p.Ala134Pro
XM_011513461.2:c.589G>C	XP_011511763.1:p.Ala197Pro
XM_017008163.1:c.-165G>C	XP_016863652.1:n.-165G>C