Canonical Allele Identifier: CA220502

Gene: IDUA

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002945G>C , CM000666.2:g.1002945G>C	GRCh38
NC_000004.11:g.996733G>C , CM000666.1:g.996733G>C	GRCh37
NC_000004.10:g.986733G>C	NCBI36
NG_008103.1:g.20949G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1402+1G>C	ENSP00000247933.4:n.1402+1G>C
ENST00000514224.2:c.1402+1G>C MANE Select	ENSP00000425081.2:n.1402+1G>C
ENST00000652070.1:n.1458+1G>C
ENST00000247933.8:c.1402+1G>C	ENSP00000247933.4:n.1402+1G>C
ENST00000502829.1:n.204+1G>C
ENST00000514224.1:c.1006+1G>C	ENSP00000425081.1:n.1006+1G>C
ENST00000514698.5:n.1509+1G>C
NM_000203.4:c.1402+1G>C	NP_000194.2:n.1402+1G>C
NR_110313.1:n.1490+1G>C
XM_006713882.2:c.1006+1G>C	XP_006713945.1:n.1006+1G>C
XM_011513459.1:c.1468+1G>C	XP_011511761.1:n.1468+1G>C
XM_011513460.1:c.1261+1G>C	XP_011511762.1:n.1261+1G>C
XM_011513461.1:c.1195+1G>C	XP_011511763.1:n.1195+1G>C
XM_011513462.1:c.1114+1G>C	XP_011511764.1:n.1114+1G>C
XM_011513463.1:c.1114+1G>C	XP_011511765.1:n.1114+1G>C
XR_924947.1:n.1471+1G>C
NM_000203.5:c.1402+1G>C MANE Select	NP_000194.2:n.1402+1G>C
NM_001363576.1:c.1006+1G>C	NP_001350505.1:n.1006+1G>C
XM_011513461.2:c.1195+1G>C	XP_011511763.1:n.1195+1G>C
XM_017008163.1:c.442+1G>C	XP_016863652.1:n.442+1G>C