Canonical Allele Identifier: CA355946098

Gene: IDUA SLC26A1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.987828C>T , CM000666.2:g.987828C>T	GRCh38
NC_000004.11:g.981616C>T , CM000666.1:g.981616C>T	GRCh37
NC_000004.10:g.971616C>T	NCBI36
NG_008103.1:g.5832C>T
NG_033042.1:g.10609G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000203.5:c.178C>T (IDUA) MANE Select	NP_000194.2:p.Gln60Ter
NM_022042.4:c.*1005G>A (SLC26A1) MANE Select	NP_071325.2:n.*1005G>A
ENST00000398516.3:c.*1005G>A (SLC26A1) MANE Select	ENSP00000381528.2:n.*1005G>A
ENST00000514224.2:c.178C>T (IDUA) MANE Select	ENSP00000425081.2:p.Gln60Ter
NM_000203.4:c.178C>T (IDUA)	NP_000194.2:p.Gln60Ter
NM_022042.3:c.*1005G>A (SLC26A1)	NP_071325.2:n.*1005G>A
NM_134425.2:c.576+3300G>A (SLC26A1)	NP_602297.1:n.576+3300G>A
NM_134425.3:c.576+3300G>A (SLC26A1)	NP_602297.1:n.576+3300G>A
NM_134425.4:c.576+3300G>A (SLC26A1)	NP_602297.1:n.576+3300G>A
NM_213613.3:c.*1005G>A (SLC26A1)	NP_998778.1:n.*1005G>A
NM_213613.4:c.*1005G>A (SLC26A1)	NP_998778.1:n.*1005G>A
NR_110313.1:n.266C>T (IDUA)
ENST00000247933.8:c.178C>T (IDUA)	ENSP00000247933.4:p.Gln60Ter
ENST00000247933.9:c.178C>T (IDUA)	ENSP00000247933.4:p.Gln60Ter
ENST00000361661.6:c.*1005G>A (SLC26A1)	ENSP00000354721.2:n.*1005G>A
ENST00000398520.6:c.576+3300G>A (SLC26A1)	ENSP00000381532.2:n.576+3300G>A
ENST00000502910.5:c.158+586C>T (IDUA)	ENSP00000422952.1:n.158+586C>T
ENST00000504568.5:c.176C>T (IDUA)
ENST00000506561.5:n.187C>T (IDUA)
ENST00000508168.5:n.177+586C>T (IDUA)
ENST00000514698.5:n.199+586C>T (IDUA)
ENST00000622731.4:c.576+3300G>A (SLC26A1)	ENSP00000483506.1:n.576+3300G>A
XM_006713856.2:c.*1005G>A (SLC26A1)	XP_006713919.1:n.*1005G>A
XM_011513459.1:c.158+586C>T (IDUA)	XP_011511761.1:n.158+586C>T
XM_011513460.1:c.158+586C>T (IDUA)	XP_011511762.1:n.158+586C>T
XM_017008163.1:c.-1289C>T (IDUA)	XP_016863652.1:n.-1289C>T
XR_924947.1:n.247C>T (IDUA)