Canonical Allele Identifier: CA800604090

Gene: IDUA SLC26A1

Linked Data

• dbSNP Id: rs1171590893
• gnomAD v4: 4-987679-T-C
• MyVariant Identifiers: chr4:g.981467T>C (hg19) ; chr4:g.987679T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.987679T>C , CM000666.2:g.987679T>C	GRCh38
NC_000004.11:g.981467T>C , CM000666.1:g.981467T>C	GRCh37
NC_000004.10:g.971467T>C	NCBI36
NG_008103.1:g.5683T>C
NG_033042.1:g.10758A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000247933.9:c.159-130T>C (IDUA)	ENSP00000247933.4:n.159-130T>C
ENST00000398516.3:c.*1154A>G (SLC26A1) MANE Select	ENSP00000381528.2:n.*1154A>G
ENST00000514224.2:c.159-130T>C (IDUA) MANE Select	ENSP00000425081.2:n.159-130T>C
ENST00000247933.8:c.159-130T>C (IDUA)	ENSP00000247933.4:n.159-130T>C
ENST00000361661.6:c.*1154A>G (SLC26A1)	ENSP00000354721.2:n.*1154A>G
ENST00000398520.6:c.576+3449A>G (SLC26A1)	ENSP00000381532.2:n.576+3449A>G
ENST00000502910.5:c.158+437T>C (IDUA)	ENSP00000422952.1:n.158+437T>C
ENST00000504568.5:c.157-130T>C (IDUA)
ENST00000506561.5:n.168-130T>C (IDUA)
ENST00000508168.5:n.177+437T>C (IDUA)
ENST00000514698.5:n.199+437T>C (IDUA)
ENST00000622731.4:c.576+3449A>G (SLC26A1)	ENSP00000483506.1:n.576+3449A>G
NM_000203.4:c.159-130T>C (IDUA)	NP_000194.2:n.159-130T>C
NM_022042.3:c.*1154A>G (SLC26A1)	NP_071325.2:n.*1154A>G
NM_134425.2:c.576+3449A>G (SLC26A1)	NP_602297.1:n.576+3449A>G
NM_213613.3:c.*1154A>G (SLC26A1)	NP_998778.1:n.*1154A>G
NR_110313.1:n.247-130T>C (IDUA)
XM_006713856.2:c.*1154A>G (SLC26A1)	XP_006713919.1:n.*1154A>G
XM_011513459.1:c.158+437T>C (IDUA)	XP_011511761.1:n.158+437T>C
XM_011513460.1:c.158+437T>C (IDUA)	XP_011511762.1:n.158+437T>C
XR_924947.1:n.228-130T>C (IDUA)
NM_000203.5:c.159-130T>C (IDUA) MANE Select	NP_000194.2:n.159-130T>C
XM_017008163.1:c.-1308-130T>C (IDUA)	XP_016863652.1:n.-1308-130T>C
NM_022042.4:c.*1154A>G (SLC26A1) MANE Select	NP_071325.2:n.*1154A>G
NM_134425.3:c.576+3449A>G (SLC26A1)	NP_602297.1:n.576+3449A>G
NM_213613.4:c.*1154A>G (SLC26A1)	NP_998778.1:n.*1154A>G
NM_134425.4:c.576+3449A>G (SLC26A1)	NP_602297.1:n.576+3449A>G