Canonical Allele Identifier: CA2801910

Gene: IDUA

Linked Data

• dbSNP Id: rs746311088
• ExAC: 4:994670 G / C
• gnomAD v2: 4-994670-G-C
• gnomAD v3: 4-1000882-G-C
• gnomAD v4: 4-1000882-G-C
• MyVariant Identifiers: chr4:g.994670G>C (hg19) ; chr4:g.1000882G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1000882G>C , CM000666.2:g.1000882G>C	GRCh38
NC_000004.11:g.994670G>C , CM000666.1:g.994670G>C	GRCh37
NC_000004.10:g.984670G>C	NCBI36
NG_008103.1:g.18886G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000247933.9:c.386G>C	ENSP00000247933.4:p.Gly129Ala
ENST00000514224.2:c.386G>C MANE Select	ENSP00000425081.2:p.Gly129Ala
ENST00000652070.1:n.442G>C
ENST00000247933.8:c.386G>C	ENSP00000247933.4:p.Gly129Ala
ENST00000502910.5:c.245G>C	ENSP00000422952.1:p.Gly82Ala
ENST00000504568.5:c.346G>C
ENST00000506561.5:n.395G>C
ENST00000508168.5:n.264G>C
ENST00000509948.5:c.179G>C	ENSP00000424227.1:p.Gly60Ala
ENST00000514192.5:c.203G>C	ENSP00000423685.1:p.Gly68Ala
ENST00000514224.1:c.-11G>C	ENSP00000425081.1:n.-11G>C
ENST00000514698.5:n.286G>C
NM_000203.4:c.386G>C	NP_000194.2:p.Gly129Ala
NR_110313.1:n.474G>C
XM_006713882.2:c.-11G>C	XP_006713945.1:n.-11G>C
XM_011513459.1:c.245G>C	XP_011511761.1:p.Gly82Ala
XM_011513460.1:c.245G>C	XP_011511762.1:p.Gly82Ala
XM_011513461.1:c.179G>C	XP_011511763.1:p.Gly60Ala
XM_011513462.1:c.98G>C	XP_011511764.1:p.Gly33Ala
XM_011513463.1:c.98G>C	XP_011511765.1:p.Gly33Ala
XR_924947.1:n.455G>C
NM_000203.5:c.386G>C MANE Select	NP_000194.2:p.Gly129Ala
NM_001363576.1:c.-11G>C	NP_001350505.1:n.-11G>C
XM_011513461.2:c.179G>C	XP_011511763.1:p.Gly60Ala
XM_017008163.1:c.-1081G>C	XP_016863652.1:n.-1081G>C