Canonical Allele Identifier: CA355962994

Gene: IDUA

Linked Data

• gnomAD v4: 4-1002293-C-G
• MyVariant Identifiers: chr4:g.996081C>G (hg19) ; chr4:g.1002293C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002293C>G , CM000666.2:g.1002293C>G	GRCh38
NC_000004.11:g.996081C>G , CM000666.1:g.996081C>G	GRCh37
NC_000004.10:g.986081C>G	NCBI36
NG_008103.1:g.20297C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.997C>G	ENSP00000247933.4:p.Leu333Val
ENST00000514224.2:c.997C>G MANE Select	ENSP00000425081.2:p.Leu333Val
ENST00000652070.1:n.1053C>G
ENST00000247933.8:c.997C>G	ENSP00000247933.4:p.Leu333Val
ENST00000514224.1:c.601C>G	ENSP00000425081.1:p.Leu201Val
ENST00000514698.5:n.1104C>G
NM_000203.4:c.997C>G	NP_000194.2:p.Leu333Val
NR_110313.1:n.1085C>G
XM_006713882.2:c.601C>G	XP_006713945.1:p.Leu201Val
XM_011513459.1:c.1063C>G	XP_011511761.1:p.Leu355Val
XM_011513460.1:c.856C>G	XP_011511762.1:p.Leu286Val
XM_011513461.1:c.790C>G	XP_011511763.1:p.Leu264Val
XM_011513462.1:c.709C>G	XP_011511764.1:p.Leu237Val
XM_011513463.1:c.709C>G	XP_011511765.1:p.Leu237Val
XR_924947.1:n.1066C>G
NM_000203.5:c.997C>G MANE Select	NP_000194.2:p.Leu333Val
NM_001363576.1:c.601C>G	NP_001350505.1:p.Leu201Val
XM_011513461.2:c.790C>G	XP_011511763.1:p.Leu264Val
XM_017008163.1:c.37C>G	XP_016863652.1:p.Leu13Val