Canonical Allele Identifier: CA355963587

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.996551G>C (hg19) ; chr4:g.1002763G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1002763G>C , CM000666.2:g.1002763G>C	GRCh38
NC_000004.11:g.996551G>C , CM000666.1:g.996551G>C	GRCh37
NC_000004.10:g.986551G>C	NCBI36
NG_008103.1:g.20767G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1221G>C	ENSP00000247933.4:p.Gln407His
ENST00000514224.2:c.1221G>C MANE Select	ENSP00000425081.2:p.Gln407His
ENST00000652070.1:n.1277G>C
ENST00000247933.8:c.1221G>C	ENSP00000247933.4:p.Gln407His
ENST00000502829.1:n.23G>C
ENST00000514224.1:c.825G>C	ENSP00000425081.1:p.Gln275His
ENST00000514698.5:n.1328G>C
NM_000203.4:c.1221G>C	NP_000194.2:p.Gln407His
NR_110313.1:n.1309G>C
XM_006713882.2:c.825G>C	XP_006713945.1:p.Gln275His
XM_011513459.1:c.1287G>C	XP_011511761.1:p.Gln429His
XM_011513460.1:c.1080G>C	XP_011511762.1:p.Gln360His
XM_011513461.1:c.1014G>C	XP_011511763.1:p.Gln338His
XM_011513462.1:c.933G>C	XP_011511764.1:p.Gln311His
XM_011513463.1:c.933G>C	XP_011511765.1:p.Gln311His
XR_924947.1:n.1290G>C
NM_000203.5:c.1221G>C MANE Select	NP_000194.2:p.Gln407His
NM_001363576.1:c.825G>C	NP_001350505.1:p.Gln275His
XM_011513461.2:c.1014G>C	XP_011511763.1:p.Gln338His
XM_017008163.1:c.261G>C	XP_016863652.1:p.Gln87His