Canonical Allele Identifier: CA438057730

Gene: IDUA

Linked Data

• gnomAD v4: 4-1002799-C-T
• MyVariant Identifiers: chr4:g.996587C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002799C>T , CM000666.2:g.1002799C>T	GRCh38
NC_000004.11:g.996587C>T , CM000666.1:g.996587C>T	GRCh37
NC_000004.10:g.986587C>T	NCBI36
NG_008103.1:g.20803C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1257C>T	ENSP00000247933.4:p.Gly419=
ENST00000514224.2:c.1257C>T MANE Select	ENSP00000425081.2:p.Gly419=
ENST00000652070.1:n.1313C>T
ENST00000247933.8:c.1257C>T	ENSP00000247933.4:p.Gly419=
ENST00000502829.1:n.59C>T
ENST00000514224.1:c.861C>T	ENSP00000425081.1:p.Gly287=
ENST00000514698.5:n.1364C>T
NM_000203.4:c.1257C>T	NP_000194.2:p.Gly419=
NR_110313.1:n.1345C>T
XM_006713882.2:c.861C>T	XP_006713945.1:p.Gly287=
XM_011513459.1:c.1323C>T	XP_011511761.1:p.Gly441=
XM_011513460.1:c.1116C>T	XP_011511762.1:p.Gly372=
XM_011513461.1:c.1050C>T	XP_011511763.1:p.Gly350=
XM_011513462.1:c.969C>T	XP_011511764.1:p.Gly323=
XM_011513463.1:c.969C>T	XP_011511765.1:p.Gly323=
XR_924947.1:n.1326C>T
NM_000203.5:c.1257C>T MANE Select	NP_000194.2:p.Gly419=
NM_001363576.1:c.861C>T	NP_001350505.1:p.Gly287=
XM_011513461.2:c.1050C>T	XP_011511763.1:p.Gly350=
XM_017008163.1:c.297C>T	XP_016863652.1:p.Gly99=