Canonical Allele Identifier: CA355962260

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.995661C>G (hg19) ; chr4:g.1001873C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001873C>G , CM000666.2:g.1001873C>G	GRCh38
NC_000004.11:g.995661C>G , CM000666.1:g.995661C>G	GRCh37
NC_000004.10:g.985661C>G	NCBI36
NG_008103.1:g.19877C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.784C>G	ENSP00000247933.4:p.His262Asp
ENST00000514224.2:c.784C>G MANE Select	ENSP00000425081.2:p.His262Asp
ENST00000652070.1:n.840C>G
ENST00000247933.8:c.784C>G	ENSP00000247933.4:p.His262Asp
ENST00000502910.5:c.643C>G	ENSP00000422952.1:p.His215Asp
ENST00000514192.5:c.601C>G	ENSP00000423685.1:p.His201Asp
ENST00000514224.1:c.388C>G	ENSP00000425081.1:p.His130Asp
ENST00000514698.5:n.684C>G
NM_000203.4:c.784C>G	NP_000194.2:p.His262Asp
NR_110313.1:n.872C>G
XM_006713882.2:c.388C>G	XP_006713945.1:p.His130Asp
XM_011513459.1:c.643C>G	XP_011511761.1:p.His215Asp
XM_011513460.1:c.643C>G	XP_011511762.1:p.His215Asp
XM_011513461.1:c.577C>G	XP_011511763.1:p.His193Asp
XM_011513462.1:c.496C>G	XP_011511764.1:p.His166Asp
XM_011513463.1:c.496C>G	XP_011511765.1:p.His166Asp
XR_924947.1:n.853C>G
NM_000203.5:c.784C>G MANE Select	NP_000194.2:p.His262Asp
NM_001363576.1:c.388C>G	NP_001350505.1:p.His130Asp
XM_011513461.2:c.577C>G	XP_011511763.1:p.His193Asp
XM_017008163.1:c.-177C>G	XP_016863652.1:n.-177C>G