Canonical Allele Identifier: CA784303865

Gene: IDUA

Linked Data

• dbSNP Id: rs1313447236
• gnomAD v3: 4-1001929-C-G
• gnomAD v4: 4-1001929-C-G
• MyVariant Identifiers: chr4:g.995717C>G (hg19) ; chr4:g.1001929C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001929C>G , CM000666.2:g.1001929C>G	GRCh38
NC_000004.11:g.995717C>G , CM000666.1:g.995717C>G	GRCh37
NC_000004.10:g.985717C>G	NCBI36
NG_008103.1:g.19933C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.792+48C>G	ENSP00000247933.4:n.792+48C>G
ENST00000514224.2:c.792+48C>G MANE Select	ENSP00000425081.2:n.792+48C>G
ENST00000652070.1:n.848+48C>G
ENST00000247933.8:c.792+48C>G	ENSP00000247933.4:n.792+48C>G
ENST00000502910.5:c.651+48C>G	ENSP00000422952.1:n.651+48C>G
ENST00000514192.5:c.609+48C>G	ENSP00000423685.1:n.609+48C>G
ENST00000514224.1:c.396+48C>G	ENSP00000425081.1:n.396+48C>G
ENST00000514698.5:n.740C>G
NM_000203.4:c.792+48C>G	NP_000194.2:n.792+48C>G
NR_110313.1:n.880+48C>G
XM_006713882.2:c.396+48C>G	XP_006713945.1:n.396+48C>G
XM_011513459.1:c.699C>G	XP_011511761.1:p.Arg233=
XM_011513460.1:c.651+48C>G	XP_011511762.1:n.651+48C>G
XM_011513461.1:c.585+48C>G	XP_011511763.1:n.585+48C>G
XM_011513462.1:c.504+48C>G	XP_011511764.1:n.504+48C>G
XM_011513463.1:c.504+48C>G	XP_011511765.1:n.504+48C>G
XR_924947.1:n.861+48C>G
NM_000203.5:c.792+48C>G MANE Select	NP_000194.2:n.792+48C>G
NM_001363576.1:c.396+48C>G	NP_001350505.1:n.396+48C>G
XM_011513461.2:c.585+48C>G	XP_011511763.1:n.585+48C>G
XM_017008163.1:c.-169+48C>G	XP_016863652.1:n.-169+48C>G