Canonical Allele Identifier: CA355946077

Gene: IDUA SLC26A1

Linked Data

• dbSNP Id: rs1343172437
• MyVariant Identifiers: chr4:g.981613A>G (hg19) ; chr4:g.987825A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.987825A>G , CM000666.2:g.987825A>G	GRCh38
NC_000004.11:g.981613A>G , CM000666.1:g.981613A>G	GRCh37
NC_000004.10:g.971613A>G	NCBI36
NG_008103.1:g.5829A>G
NG_033042.1:g.10612T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.175A>G (IDUA)	ENSP00000247933.4:p.Ser59Gly
ENST00000398516.3:c.*1008T>C (SLC26A1) MANE Select	ENSP00000381528.2:n.*1008T>C
ENST00000514224.2:c.175A>G (IDUA) MANE Select	ENSP00000425081.2:p.Ser59Gly
ENST00000247933.8:c.175A>G (IDUA)	ENSP00000247933.4:p.Ser59Gly
ENST00000361661.6:c.*1008T>C (SLC26A1)	ENSP00000354721.2:n.*1008T>C
ENST00000398520.6:c.576+3303T>C (SLC26A1)	ENSP00000381532.2:n.576+3303T>C
ENST00000502910.5:c.158+583A>G (IDUA)	ENSP00000422952.1:n.158+583A>G
ENST00000504568.5:c.173A>G (IDUA)
ENST00000506561.5:n.184A>G (IDUA)
ENST00000508168.5:n.177+583A>G (IDUA)
ENST00000514698.5:n.199+583A>G (IDUA)
ENST00000622731.4:c.576+3303T>C (SLC26A1)	ENSP00000483506.1:n.576+3303T>C
NM_000203.4:c.175A>G (IDUA)	NP_000194.2:p.Ser59Gly
NM_022042.3:c.*1008T>C (SLC26A1)	NP_071325.2:n.*1008T>C
NM_134425.2:c.576+3303T>C (SLC26A1)	NP_602297.1:n.576+3303T>C
NM_213613.3:c.*1008T>C (SLC26A1)	NP_998778.1:n.*1008T>C
NR_110313.1:n.263A>G (IDUA)
XM_006713856.2:c.*1008T>C (SLC26A1)	XP_006713919.1:n.*1008T>C
XM_011513459.1:c.158+583A>G (IDUA)	XP_011511761.1:n.158+583A>G
XM_011513460.1:c.158+583A>G (IDUA)	XP_011511762.1:n.158+583A>G
XR_924947.1:n.244A>G (IDUA)
NM_000203.5:c.175A>G (IDUA) MANE Select	NP_000194.2:p.Ser59Gly
XM_017008163.1:c.-1292A>G (IDUA)	XP_016863652.1:n.-1292A>G
NM_022042.4:c.*1008T>C (SLC26A1) MANE Select	NP_071325.2:n.*1008T>C
NM_134425.3:c.576+3303T>C (SLC26A1)	NP_602297.1:n.576+3303T>C
NM_213613.4:c.*1008T>C (SLC26A1)	NP_998778.1:n.*1008T>C
NM_134425.4:c.576+3303T>C (SLC26A1)	NP_602297.1:n.576+3303T>C