Canonical Allele Identifier: CA438057283

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.995546C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001758C>T , CM000666.2:g.1001758C>T	GRCh38
NC_000004.11:g.995546C>T , CM000666.1:g.995546C>T	GRCh37
NC_000004.10:g.985546C>T	NCBI36
NG_008103.1:g.19762C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.669C>T	ENSP00000247933.4:p.Asp223=
ENST00000514224.2:c.669C>T MANE Select	ENSP00000425081.2:p.Asp223=
ENST00000652070.1:n.725C>T
ENST00000247933.8:c.669C>T	ENSP00000247933.4:p.Asp223=
ENST00000502910.5:c.528C>T	ENSP00000422952.1:p.Asp176=
ENST00000509948.5:c.462C>T	ENSP00000424227.1:p.Asp154=
ENST00000514192.5:c.486C>T	ENSP00000423685.1:p.Asp162=
ENST00000514224.1:c.273C>T	ENSP00000425081.1:p.Asp91=
ENST00000514698.5:n.569C>T
NM_000203.4:c.669C>T	NP_000194.2:p.Asp223=
NR_110313.1:n.757C>T
XM_006713882.2:c.273C>T	XP_006713945.1:p.Asp91=
XM_011513459.1:c.528C>T	XP_011511761.1:p.Asp176=
XM_011513460.1:c.528C>T	XP_011511762.1:p.Asp176=
XM_011513461.1:c.462C>T	XP_011511763.1:p.Asp154=
XM_011513462.1:c.381C>T	XP_011511764.1:p.Asp127=
XM_011513463.1:c.381C>T	XP_011511765.1:p.Asp127=
XR_924947.1:n.738C>T
NM_000203.5:c.669C>T MANE Select	NP_000194.2:p.Asp223=
NM_001363576.1:c.273C>T	NP_001350505.1:p.Asp91=
XM_011513461.2:c.462C>T	XP_011511763.1:p.Asp154=
XM_017008163.1:c.-292C>T	XP_016863652.1:n.-292C>T