Canonical Allele Identifier: CA355964925

Gene: IDUA

Linked Data

• gnomAD v4: 4-1003360-G-T
• MyVariant Identifiers: chr4:g.997148G>T (hg19) ; chr4:g.1003360G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003360G>T , CM000666.2:g.1003360G>T	GRCh38
NC_000004.11:g.997148G>T , CM000666.1:g.997148G>T	GRCh37
NC_000004.10:g.987148G>T	NCBI36
NG_008103.1:g.21364G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1540G>T	ENSP00000247933.4:p.Ala514Ser
ENST00000514224.2:c.1540G>T MANE Select	ENSP00000425081.2:p.Ala514Ser
ENST00000652070.1:n.1596G>T
ENST00000247933.8:c.1540G>T	ENSP00000247933.4:p.Ala514Ser
ENST00000502829.1:n.529G>T
ENST00000514224.1:c.1144G>T	ENSP00000425081.1:p.Ala382Ser
ENST00000514698.5:n.1647G>T
NM_000203.4:c.1540G>T	NP_000194.2:p.Ala514Ser
NR_110313.1:n.1628G>T
XM_006713882.2:c.1144G>T	XP_006713945.1:p.Ala382Ser
XM_011513459.1:c.1606G>T	XP_011511761.1:p.Ala536Ser
XM_011513460.1:c.1399G>T	XP_011511762.1:p.Ala467Ser
XM_011513461.1:c.1333G>T	XP_011511763.1:p.Ala445Ser
XM_011513462.1:c.1252G>T	XP_011511764.1:p.Ala418Ser
XM_011513463.1:c.1252G>T	XP_011511765.1:p.Ala418Ser
XR_924947.1:n.1796G>T
NM_000203.5:c.1540G>T MANE Select	NP_000194.2:p.Ala514Ser
NM_001363576.1:c.1144G>T	NP_001350505.1:p.Ala382Ser
XM_011513461.2:c.1333G>T	XP_011511763.1:p.Ala445Ser
XM_017008163.1:c.580G>T	XP_016863652.1:p.Ala194Ser