Canonical Allele Identifier: CA549561633
Gene: SLC2A9 HGNC NCBI

Linked Data

dbSNP Id: rs1271183325

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.9962864_9962865del , CM000666.2:g.9962864_9962865del GRCh38
NC_000004.11:g.9964488_9964489del , CM000666.1:g.9964488_9964489del GRCh37
NC_000004.10:g.9573586_9573587del NCBI36
NG_011540.1:g.82387_82388del

Transcript Alleles

HGVS Amino-acid change
ENST00000264784.8:c.681+17730_681+17731del MANE Select ENSP00000264784.3:n.681+17730_681+17731de...
ENST00000264784.7:c.681+17730_681+17731del ENSP00000264784.3:n.681+17730_681+17731de...
ENST00000309065.7:c.594+17730_594+17731del ENSP00000311383.3:n.594+17730_594+17731de...
ENST00000505104.5:n.715+17730_715+17731del
ENST00000506583.5:c.594+17730_594+17731del ENSP00000422209.1:n.594+17730_594+17731de...
NM_001001290.1:c.594+17730_594+17731del NP_001001290.1:n.594+17730_594+17731del
NM_020041.2:c.681+17730_681+17731del NP_064425.2:n.681+17730_681+17731del
XM_006713968.2:c.681+17730_681+17731del XP_006714031.1:n.681+17730_681+17731del
XM_006713969.2:c.594+17730_594+17731del XP_006714032.1:n.594+17730_594+17731del
XM_011513856.1:c.681+17730_681+17731del XP_011512158.1:n.681+17730_681+17731del
XM_011513857.1:c.594+17730_594+17731del XP_011512159.1:n.594+17730_594+17731del
XM_011513858.1:c.594+17730_594+17731del XP_011512160.1:n.594+17730_594+17731del
XM_011513859.1:c.681+17730_681+17731del XP_011512161.1:n.681+17730_681+17731del
XM_011513860.1:c.681+17730_681+17731del XP_011512162.1:n.681+17730_681+17731del
XM_011513861.1:c.681+17730_681+17731del XP_011512163.1:n.681+17730_681+17731del
XM_011513862.1:c.285+17730_285+17731del XP_011512164.1:n.285+17730_285+17731del
XM_011513863.1:c.285+17730_285+17731del XP_011512165.1:n.285+17730_285+17731del
XM_011513864.1:c.273+17730_273+17731del XP_011512166.1:n.273+17730_273+17731del
XM_011513865.1:c.681+17730_681+17731del XP_011512167.1:n.681+17730_681+17731del
XM_011513866.1:c.681+17730_681+17731del XP_011512168.1:n.681+17730_681+17731del
XM_011513867.1:c.123+17730_123+17731del XP_011512169.1:n.123+17730_123+17731del
XM_011513868.1:c.681+17730_681+17731del XP_011512170.1:n.681+17730_681+17731del
XR_925341.1:n.777+17730_777+17731del
XM_006713968.4:c.681+17730_681+17731del XP_006714031.1:n.681+17730_681+17731del
XM_011513856.3:c.681+17730_681+17731del XP_011512158.1:n.681+17730_681+17731del
XM_011513859.3:c.681+17730_681+17731del XP_011512161.1:n.681+17730_681+17731del
XM_011513860.3:c.681+17730_681+17731del XP_011512162.1:n.681+17730_681+17731del
XM_011513861.3:c.681+17730_681+17731del XP_011512163.1:n.681+17730_681+17731del
XM_011513862.3:c.285+17730_285+17731del XP_011512164.1:n.285+17730_285+17731del
XM_011513864.2:c.273+17730_273+17731del XP_011512166.1:n.273+17730_273+17731del
XM_011513865.2:c.681+17730_681+17731del XP_011512167.1:n.681+17730_681+17731del
XM_011513866.2:c.681+17730_681+17731del XP_011512168.1:n.681+17730_681+17731del
XM_011513867.3:c.123+17730_123+17731del XP_011512169.1:n.123+17730_123+17731del
XM_011513868.2:c.681+17730_681+17731del XP_011512170.1:n.681+17730_681+17731del
XM_017008457.2:c.681+17730_681+17731del XP_016863946.1:n.681+17730_681+17731del
XM_017008458.2:c.681+17730_681+17731del XP_016863947.1:n.681+17730_681+17731del
XM_017008459.1:c.219+17730_219+17731del XP_016863948.1:n.219+17730_219+17731del
XM_017008460.2:c.285+17730_285+17731del XP_016863949.1:n.285+17730_285+17731del
XM_024454150.1:c.681+17730_681+17731del XP_024309918.1:n.681+17730_681+17731del
XM_024454151.1:c.294+17730_294+17731del XP_024309919.1:n.294+17730_294+17731del
XM_024454152.1:c.681+17730_681+17731del XP_024309920.1:n.681+17730_681+17731del
XM_024454153.1:c.681+17730_681+17731del XP_024309921.1:n.681+17730_681+17731del
XR_001741290.1:n.854+17730_854+17731del
XR_001741291.1:n.854+17730_854+17731del
XR_925341.3:n.858+17730_858+17731del
NM_020041.3:c.681+17730_681+17731del MANE Select NP_064425.2:n.681+17730_681+17731del
NM_001001290.2:c.594+17730_594+17731del NP_001001290.1:n.594+17730_594+17731del