Canonical Allele Identifier: CA2669480073

Gene: IDUA

Linked Data

• gnomAD v4: 4-1001900-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001900T>G , CM000666.2:g.1001900T>G	GRCh38
NC_000004.11:g.995688T>G , CM000666.1:g.995688T>G	GRCh37
NC_000004.10:g.985688T>G	NCBI36
NG_008103.1:g.19904T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.792+19T>G	ENSP00000247933.4:n.792+19T>G
ENST00000514224.2:c.792+19T>G MANE Select	ENSP00000425081.2:n.792+19T>G
ENST00000652070.1:n.848+19T>G
ENST00000247933.8:c.792+19T>G	ENSP00000247933.4:n.792+19T>G
ENST00000502910.5:c.651+19T>G	ENSP00000422952.1:n.651+19T>G
ENST00000514192.5:c.609+19T>G	ENSP00000423685.1:n.609+19T>G
ENST00000514224.1:c.396+19T>G	ENSP00000425081.1:n.396+19T>G
ENST00000514698.5:n.711T>G
NM_000203.4:c.792+19T>G	NP_000194.2:n.792+19T>G
NR_110313.1:n.880+19T>G
XM_006713882.2:c.396+19T>G	XP_006713945.1:n.396+19T>G
XM_011513459.1:c.670T>G	XP_011511761.1:p.Ser224Ala
XM_011513460.1:c.651+19T>G	XP_011511762.1:n.651+19T>G
XM_011513461.1:c.585+19T>G	XP_011511763.1:n.585+19T>G
XM_011513462.1:c.504+19T>G	XP_011511764.1:n.504+19T>G
XM_011513463.1:c.504+19T>G	XP_011511765.1:n.504+19T>G
XR_924947.1:n.861+19T>G
NM_000203.5:c.792+19T>G MANE Select	NP_000194.2:n.792+19T>G
NM_001363576.1:c.396+19T>G	NP_001350505.1:n.396+19T>G
XM_011513461.2:c.585+19T>G	XP_011511763.1:n.585+19T>G
XM_017008163.1:c.-169+19T>G	XP_016863652.1:n.-169+19T>G