Canonical Allele Identifier: CA355963003

Gene: IDUA

Linked Data

• gnomAD v4: 4-1002296-C-G
• MyVariant Identifiers: chr4:g.996084C>G (hg19) ; chr4:g.1002296C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002296C>G , CM000666.2:g.1002296C>G	GRCh38
NC_000004.11:g.996084C>G , CM000666.1:g.996084C>G	GRCh37
NC_000004.10:g.986084C>G	NCBI36
NG_008103.1:g.20300C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1000C>G	ENSP00000247933.4:p.Leu334Val
ENST00000514224.2:c.1000C>G MANE Select	ENSP00000425081.2:p.Leu334Val
ENST00000652070.1:n.1056C>G
ENST00000247933.8:c.1000C>G	ENSP00000247933.4:p.Leu334Val
ENST00000514224.1:c.604C>G	ENSP00000425081.1:p.Leu202Val
ENST00000514698.5:n.1107C>G
NM_000203.4:c.1000C>G	NP_000194.2:p.Leu334Val
NR_110313.1:n.1088C>G
XM_006713882.2:c.604C>G	XP_006713945.1:p.Leu202Val
XM_011513459.1:c.1066C>G	XP_011511761.1:p.Leu356Val
XM_011513460.1:c.859C>G	XP_011511762.1:p.Leu287Val
XM_011513461.1:c.793C>G	XP_011511763.1:p.Leu265Val
XM_011513462.1:c.712C>G	XP_011511764.1:p.Leu238Val
XM_011513463.1:c.712C>G	XP_011511765.1:p.Leu238Val
XR_924947.1:n.1069C>G
NM_000203.5:c.1000C>G MANE Select	NP_000194.2:p.Leu334Val
NM_001363576.1:c.604C>G	NP_001350505.1:p.Leu202Val
XM_011513461.2:c.793C>G	XP_011511763.1:p.Leu265Val
XM_017008163.1:c.40C>G	XP_016863652.1:p.Leu14Val