Canonical Allele Identifier: CA1437756782
Gene: SLC2A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.9920446C= , CM000666.2:g.9920446C= GRCh38
NC_000004.11:g.9922070C= , CM000666.1:g.9922070C= GRCh37
NC_000004.10:g.9531168C= NCBI36
NG_011540.1:g.124803G=

Transcript Alleles

HGVS Amino-acid change
ENST00000264784.8:c.941G= MANE Select ENSP00000264784.3:p.Arg314=
ENST00000264784.7:c.941G= ENSP00000264784.3:p.Arg314=
ENST00000309065.7:c.854G= ENSP00000311383.3:p.Arg285=
ENST00000505104.5:n.975G=
ENST00000506583.5:c.854G= ENSP00000422209.1:p.Arg285=
NM_001001290.1:c.854G= NP_001001290.1:p.Arg285=
NM_020041.2:c.941G= NP_064425.2:p.Arg314=
XM_006713968.2:c.941G= XP_006714031.1:p.Arg314=
XM_006713969.2:c.854G= XP_006714032.1:p.Arg285=
XM_011513856.1:c.941G= XP_011512158.1:p.Arg314=
XM_011513857.1:c.854G= XP_011512159.1:p.Arg285=
XM_011513858.1:c.854G= XP_011512160.1:p.Arg285=
XM_011513859.1:c.941G= XP_011512161.1:p.Arg314=
XM_011513860.1:c.941G= XP_011512162.1:p.Arg314=
XM_011513861.1:c.941G= XP_011512163.1:p.Arg314=
XM_011513862.1:c.545G= XP_011512164.1:p.Arg182=
XM_011513863.1:c.545G= XP_011512165.1:p.Arg182=
XM_011513864.1:c.533G= XP_011512166.1:p.Arg178=
XM_011513865.1:c.941G= XP_011512167.1:p.Arg314=
XM_011513866.1:c.941G= XP_011512168.1:p.Arg314=
XM_011513867.1:c.383G= XP_011512169.1:p.Arg128=
XM_011513868.1:c.941G= XP_011512170.1:p.Arg314=
XR_925341.1:n.1037G=
XM_006713968.4:c.941G= XP_006714031.1:p.Arg314=
XM_011513856.3:c.941G= XP_011512158.1:p.Arg314=
XM_011513859.3:c.941G= XP_011512161.1:p.Arg314=
XM_011513860.3:c.941G= XP_011512162.1:p.Arg314=
XM_011513861.3:c.941G= XP_011512163.1:p.Arg314=
XM_011513862.3:c.545G= XP_011512164.1:p.Arg182=
XM_011513864.2:c.533G= XP_011512166.1:p.Arg178=
XM_011513865.2:c.941G= XP_011512167.1:p.Arg314=
XM_011513866.2:c.941G= XP_011512168.1:p.Arg314=
XM_011513867.3:c.383G= XP_011512169.1:p.Arg128=
XM_011513868.2:c.941G= XP_011512170.1:p.Arg314=
XM_017008457.2:c.941G= XP_016863946.1:p.Arg314=
XM_017008458.2:c.941G= XP_016863947.1:p.Arg314=
XM_017008459.1:c.479G= XP_016863948.1:p.Arg160=
XM_017008460.2:c.545G= XP_016863949.1:p.Arg182=
XM_024454150.1:c.941G= XP_024309918.1:p.Arg314=
XM_024454151.1:c.554G= XP_024309919.1:p.Arg185=
XM_024454152.1:c.941G= XP_024309920.1:p.Arg314=
XM_024454153.1:c.941G= XP_024309921.1:p.Arg314=
XR_001741290.1:n.1114G=
XR_001741291.1:n.1114G=
XR_925341.3:n.1118G=
NM_020041.3:c.941G= MANE Select NP_064425.2:p.Arg314=
NM_001001290.2:c.854G= NP_001001290.1:p.Arg285=