Canonical Allele Identifier: CA1437771305

Gene: SLC2A9

Linked Data

• dbSNP Id: rs1749807519

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.9949479_9949483dup , CM000666.2:g.9949479_9949483dup	GRCh38
NC_000004.11:g.9951103_9951107dup , CM000666.1:g.9951103_9951107dup	GRCh37
NC_000004.10:g.9560201_9560205dup	NCBI36
NG_011540.1:g.95767_95771dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000264784.8:c.682-7437_682-7433dup MANE Select	ENSP00000264784.3:n.682-7437_682-7433dup
ENST00000264784.7:c.682-7437_682-7433dup	ENSP00000264784.3:n.682-7437_682-7433dup
ENST00000309065.7:c.595-7437_595-7433dup	ENSP00000311383.3:n.595-7437_595-7433dup
ENST00000505104.5:n.716-7437_716-7433dup
ENST00000506583.5:c.595-7437_595-7433dup	ENSP00000422209.1:n.595-7437_595-7433dup
NM_001001290.1:c.595-7437_595-7433dup	NP_001001290.1:n.595-7437_595-7433dup
NM_020041.2:c.682-7437_682-7433dup	NP_064425.2:n.682-7437_682-7433dup
XM_006713968.2:c.682-7437_682-7433dup	XP_006714031.1:n.682-7437_682-7433dup
XM_006713969.2:c.595-7437_595-7433dup	XP_006714032.1:n.595-7437_595-7433dup
XM_011513856.1:c.682-7437_682-7433dup	XP_011512158.1:n.682-7437_682-7433dup
XM_011513857.1:c.595-7437_595-7433dup	XP_011512159.1:n.595-7437_595-7433dup
XM_011513858.1:c.595-7437_595-7433dup	XP_011512160.1:n.595-7437_595-7433dup
XM_011513859.1:c.682-7437_682-7433dup	XP_011512161.1:n.682-7437_682-7433dup
XM_011513860.1:c.682-7437_682-7433dup	XP_011512162.1:n.682-7437_682-7433dup
XM_011513861.1:c.682-7437_682-7433dup	XP_011512163.1:n.682-7437_682-7433dup
XM_011513862.1:c.286-7437_286-7433dup	XP_011512164.1:n.286-7437_286-7433dup
XM_011513863.1:c.286-7437_286-7433dup	XP_011512165.1:n.286-7437_286-7433dup
XM_011513864.1:c.274-7437_274-7433dup	XP_011512166.1:n.274-7437_274-7433dup
XM_011513865.1:c.682-7437_682-7433dup	XP_011512167.1:n.682-7437_682-7433dup
XM_011513866.1:c.682-7437_682-7433dup	XP_011512168.1:n.682-7437_682-7433dup
XM_011513867.1:c.124-7437_124-7433dup	XP_011512169.1:n.124-7437_124-7433dup
XM_011513868.1:c.682-7437_682-7433dup	XP_011512170.1:n.682-7437_682-7433dup
XR_925341.1:n.778-7437_778-7433dup
XM_006713968.4:c.682-7437_682-7433dup	XP_006714031.1:n.682-7437_682-7433dup
XM_011513856.3:c.682-7437_682-7433dup	XP_011512158.1:n.682-7437_682-7433dup
XM_011513859.3:c.682-7437_682-7433dup	XP_011512161.1:n.682-7437_682-7433dup
XM_011513860.3:c.682-7437_682-7433dup	XP_011512162.1:n.682-7437_682-7433dup
XM_011513861.3:c.682-7437_682-7433dup	XP_011512163.1:n.682-7437_682-7433dup
XM_011513862.3:c.286-7437_286-7433dup	XP_011512164.1:n.286-7437_286-7433dup
XM_011513864.2:c.274-7437_274-7433dup	XP_011512166.1:n.274-7437_274-7433dup
XM_011513865.2:c.682-7437_682-7433dup	XP_011512167.1:n.682-7437_682-7433dup
XM_011513866.2:c.682-7437_682-7433dup	XP_011512168.1:n.682-7437_682-7433dup
XM_011513867.3:c.124-7437_124-7433dup	XP_011512169.1:n.124-7437_124-7433dup
XM_011513868.2:c.682-7437_682-7433dup	XP_011512170.1:n.682-7437_682-7433dup
XM_017008457.2:c.682-7437_682-7433dup	XP_016863946.1:n.682-7437_682-7433dup
XM_017008458.2:c.682-7437_682-7433dup	XP_016863947.1:n.682-7437_682-7433dup
XM_017008459.1:c.220-7437_220-7433dup	XP_016863948.1:n.220-7437_220-7433dup
XM_017008460.2:c.286-7437_286-7433dup	XP_016863949.1:n.286-7437_286-7433dup
XM_024454150.1:c.682-7437_682-7433dup	XP_024309918.1:n.682-7437_682-7433dup
XM_024454151.1:c.295-7437_295-7433dup	XP_024309919.1:n.295-7437_295-7433dup
XM_024454152.1:c.682-7437_682-7433dup	XP_024309920.1:n.682-7437_682-7433dup
XM_024454153.1:c.682-7437_682-7433dup	XP_024309921.1:n.682-7437_682-7433dup
XR_001741290.1:n.855-7437_855-7433dup
XR_001741291.1:n.855-7437_855-7433dup
XR_925341.3:n.859-7437_859-7433dup
NM_020041.3:c.682-7437_682-7433dup MANE Select	NP_064425.2:n.682-7437_682-7433dup
NM_001001290.2:c.595-7437_595-7433dup	NP_001001290.1:n.595-7437_595-7433dup