Canonical Allele Identifier: CA355962218

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.995638T>A (hg19) ; chr4:g.1001850T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001850T>A , CM000666.2:g.1001850T>A	GRCh38
NC_000004.11:g.995638T>A , CM000666.1:g.995638T>A	GRCh37
NC_000004.10:g.985638T>A	NCBI36
NG_008103.1:g.19854T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.761T>A	ENSP00000247933.4:p.Val254Glu
ENST00000514224.2:c.761T>A MANE Select	ENSP00000425081.2:p.Val254Glu
ENST00000652070.1:n.817T>A
ENST00000247933.8:c.761T>A	ENSP00000247933.4:p.Val254Glu
ENST00000502910.5:c.620T>A	ENSP00000422952.1:p.Val207Glu
ENST00000514192.5:c.578T>A	ENSP00000423685.1:p.Val193Glu
ENST00000514224.1:c.365T>A	ENSP00000425081.1:p.Val122Glu
ENST00000514698.5:n.661T>A
NM_000203.4:c.761T>A	NP_000194.2:p.Val254Glu
NR_110313.1:n.849T>A
XM_006713882.2:c.365T>A	XP_006713945.1:p.Val122Glu
XM_011513459.1:c.620T>A	XP_011511761.1:p.Val207Glu
XM_011513460.1:c.620T>A	XP_011511762.1:p.Val207Glu
XM_011513461.1:c.554T>A	XP_011511763.1:p.Val185Glu
XM_011513462.1:c.473T>A	XP_011511764.1:p.Val158Glu
XM_011513463.1:c.473T>A	XP_011511765.1:p.Val158Glu
XR_924947.1:n.830T>A
NM_000203.5:c.761T>A MANE Select	NP_000194.2:p.Val254Glu
NM_001363576.1:c.365T>A	NP_001350505.1:p.Val122Glu
XM_011513461.2:c.554T>A	XP_011511763.1:p.Val185Glu
XM_017008163.1:c.-200T>A	XP_016863652.1:n.-200T>A