Canonical Allele Identifier: CA355962675

Gene: IDUA

Linked Data

• gnomAD v4: 4-1002120-C-G
• MyVariant Identifiers: chr4:g.995908C>G (hg19) ; chr4:g.1002120C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002120C>G , CM000666.2:g.1002120C>G	GRCh38
NC_000004.11:g.995908C>G , CM000666.1:g.995908C>G	GRCh37
NC_000004.10:g.985908C>G	NCBI36
NG_008103.1:g.20124C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000247933.9:c.931C>G	ENSP00000247933.4:p.Pro311Ala
ENST00000514224.2:c.931C>G MANE Select	ENSP00000425081.2:p.Pro311Ala
ENST00000652070.1:n.987C>G
ENST00000247933.8:c.931C>G	ENSP00000247933.4:p.Pro311Ala
ENST00000514224.1:c.535C>G	ENSP00000425081.1:p.Pro179Ala
ENST00000514698.5:n.931C>G
NM_000203.4:c.931C>G	NP_000194.2:p.Pro311Ala
NR_110313.1:n.1019C>G
XM_006713882.2:c.535C>G	XP_006713945.1:p.Pro179Ala
XM_011513459.1:c.890C>G	XP_011511761.1:p.Ala297Gly
XM_011513460.1:c.790C>G	XP_011511762.1:p.Pro264Ala
XM_011513461.1:c.724C>G	XP_011511763.1:p.Pro242Ala
XM_011513462.1:c.643C>G	XP_011511764.1:p.Pro215Ala
XM_011513463.1:c.643C>G	XP_011511765.1:p.Pro215Ala
XR_924947.1:n.1000C>G
NM_000203.5:c.931C>G MANE Select	NP_000194.2:p.Pro311Ala
NM_001363576.1:c.535C>G	NP_001350505.1:p.Pro179Ala
XM_011513461.2:c.724C>G	XP_011511763.1:p.Pro242Ala
XM_017008163.1:c.-30C>G	XP_016863652.1:n.-30C>G