Canonical Allele Identifier: CA2705264253

Gene: SLC2A9

Linked Data

• dbSNP Id: rs2110083922

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.9920443del , CM000666.2:g.9920443del	GRCh38
NC_000004.11:g.9922067del , CM000666.1:g.9922067del	GRCh37
NC_000004.10:g.9531165del	NCBI36
NG_011540.1:g.124807del

Transcript Alleles

HGVS	Amino-acid change
ENST00000264784.8:c.945del MANE Select	ENSP00000264784.3:p.Trp315CysfsTer6
ENST00000264784.7:c.945del	ENSP00000264784.3:p.Trp315CysfsTer6
ENST00000309065.7:c.858del	ENSP00000311383.3:p.Trp286CysfsTer6
ENST00000505104.5:n.979del
ENST00000506583.5:c.858del	ENSP00000422209.1:p.Trp286CysfsTer6
NM_001001290.1:c.858del	NP_001001290.1:p.Trp286CysfsTer6
NM_020041.2:c.945del	NP_064425.2:p.Trp315CysfsTer6
XM_006713968.2:c.945del	XP_006714031.1:p.Trp315CysfsTer6
XM_006713969.2:c.858del	XP_006714032.1:p.Trp286CysfsTer6
XM_011513856.1:c.945del	XP_011512158.1:p.Trp315CysfsTer6
XM_011513857.1:c.858del	XP_011512159.1:p.Trp286CysfsTer6
XM_011513858.1:c.858del	XP_011512160.1:p.Trp286CysfsTer6
XM_011513859.1:c.945del	XP_011512161.1:p.Trp315CysfsTer6
XM_011513860.1:c.945del	XP_011512162.1:p.Trp315CysfsTer6
XM_011513861.1:c.945del	XP_011512163.1:p.Trp315CysfsTer6
XM_011513862.1:c.549del	XP_011512164.1:p.Trp183CysfsTer6
XM_011513863.1:c.549del	XP_011512165.1:p.Trp183CysfsTer6
XM_011513864.1:c.537del	XP_011512166.1:p.Trp179CysfsTer6
XM_011513865.1:c.945del	XP_011512167.1:p.Trp315CysfsTer6
XM_011513866.1:c.945del	XP_011512168.1:p.Trp315CysfsTer6
XM_011513867.1:c.387del	XP_011512169.1:p.Trp129CysfsTer6
XM_011513868.1:c.945del	XP_011512170.1:p.Trp315CysfsTer6
XR_925341.1:n.1041del
XM_006713968.4:c.945del	XP_006714031.1:p.Trp315CysfsTer6
XM_011513856.3:c.945del	XP_011512158.1:p.Trp315CysfsTer6
XM_011513859.3:c.945del	XP_011512161.1:p.Trp315CysfsTer6
XM_011513860.3:c.945del	XP_011512162.1:p.Trp315CysfsTer6
XM_011513861.3:c.945del	XP_011512163.1:p.Trp315CysfsTer6
XM_011513862.3:c.549del	XP_011512164.1:p.Trp183CysfsTer6
XM_011513864.2:c.537del	XP_011512166.1:p.Trp179CysfsTer6
XM_011513865.2:c.945del	XP_011512167.1:p.Trp315CysfsTer6
XM_011513866.2:c.945del	XP_011512168.1:p.Trp315CysfsTer6
XM_011513867.3:c.387del	XP_011512169.1:p.Trp129CysfsTer6
XM_011513868.2:c.945del	XP_011512170.1:p.Trp315CysfsTer6
XM_017008457.2:c.945del	XP_016863946.1:p.Trp315CysfsTer6
XM_017008458.2:c.945del	XP_016863947.1:p.Trp315CysfsTer6
XM_017008459.1:c.483del	XP_016863948.1:p.Trp161CysfsTer6
XM_017008460.2:c.549del	XP_016863949.1:p.Trp183CysfsTer6
XM_024454150.1:c.945del	XP_024309918.1:p.Trp315CysfsTer6
XM_024454151.1:c.558del	XP_024309919.1:p.Trp186CysfsTer6
XM_024454152.1:c.945del	XP_024309920.1:p.Trp315CysfsTer6
XM_024454153.1:c.945del	XP_024309921.1:p.Trp315CysfsTer6
XR_001741290.1:n.1118del
XR_001741291.1:n.1118del
XR_925341.3:n.1122del
NM_020041.3:c.945del MANE Select	NP_064425.2:p.Trp315CysfsTer6
NM_001001290.2:c.858del	NP_001001290.1:p.Trp286CysfsTer6