Canonical Allele Identifier: CA1437771872

Gene: SLC2A9

Linked Data

• dbSNP Id: rs1749933623

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.9950029_9950030del , CM000666.2:g.9950029_9950030del	GRCh38
NC_000004.11:g.9951653_9951654del , CM000666.1:g.9951653_9951654del	GRCh37
NC_000004.10:g.9560751_9560752del	NCBI36
NG_011540.1:g.95221_95222del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264784.8:c.682-7983_682-7982del MANE Select	ENSP00000264784.3:n.682-7983_682-7982del
ENST00000264784.7:c.682-7983_682-7982del	ENSP00000264784.3:n.682-7983_682-7982del
ENST00000309065.7:c.595-7983_595-7982del	ENSP00000311383.3:n.595-7983_595-7982del
ENST00000505104.5:n.716-7983_716-7982del
ENST00000506583.5:c.595-7983_595-7982del	ENSP00000422209.1:n.595-7983_595-7982del
NM_001001290.1:c.595-7983_595-7982del	NP_001001290.1:n.595-7983_595-7982del
NM_020041.2:c.682-7983_682-7982del	NP_064425.2:n.682-7983_682-7982del
XM_006713968.2:c.682-7983_682-7982del	XP_006714031.1:n.682-7983_682-7982del
XM_006713969.2:c.595-7983_595-7982del	XP_006714032.1:n.595-7983_595-7982del
XM_011513856.1:c.682-7983_682-7982del	XP_011512158.1:n.682-7983_682-7982del
XM_011513857.1:c.595-7983_595-7982del	XP_011512159.1:n.595-7983_595-7982del
XM_011513858.1:c.595-7983_595-7982del	XP_011512160.1:n.595-7983_595-7982del
XM_011513859.1:c.682-7983_682-7982del	XP_011512161.1:n.682-7983_682-7982del
XM_011513860.1:c.682-7983_682-7982del	XP_011512162.1:n.682-7983_682-7982del
XM_011513861.1:c.682-7983_682-7982del	XP_011512163.1:n.682-7983_682-7982del
XM_011513862.1:c.286-7983_286-7982del	XP_011512164.1:n.286-7983_286-7982del
XM_011513863.1:c.286-7983_286-7982del	XP_011512165.1:n.286-7983_286-7982del
XM_011513864.1:c.274-7983_274-7982del	XP_011512166.1:n.274-7983_274-7982del
XM_011513865.1:c.682-7983_682-7982del	XP_011512167.1:n.682-7983_682-7982del
XM_011513866.1:c.682-7983_682-7982del	XP_011512168.1:n.682-7983_682-7982del
XM_011513867.1:c.124-7983_124-7982del	XP_011512169.1:n.124-7983_124-7982del
XM_011513868.1:c.682-7983_682-7982del	XP_011512170.1:n.682-7983_682-7982del
XR_925341.1:n.778-7983_778-7982del
XM_006713968.4:c.682-7983_682-7982del	XP_006714031.1:n.682-7983_682-7982del
XM_011513856.3:c.682-7983_682-7982del	XP_011512158.1:n.682-7983_682-7982del
XM_011513859.3:c.682-7983_682-7982del	XP_011512161.1:n.682-7983_682-7982del
XM_011513860.3:c.682-7983_682-7982del	XP_011512162.1:n.682-7983_682-7982del
XM_011513861.3:c.682-7983_682-7982del	XP_011512163.1:n.682-7983_682-7982del
XM_011513862.3:c.286-7983_286-7982del	XP_011512164.1:n.286-7983_286-7982del
XM_011513864.2:c.274-7983_274-7982del	XP_011512166.1:n.274-7983_274-7982del
XM_011513865.2:c.682-7983_682-7982del	XP_011512167.1:n.682-7983_682-7982del
XM_011513866.2:c.682-7983_682-7982del	XP_011512168.1:n.682-7983_682-7982del
XM_011513867.3:c.124-7983_124-7982del	XP_011512169.1:n.124-7983_124-7982del
XM_011513868.2:c.682-7983_682-7982del	XP_011512170.1:n.682-7983_682-7982del
XM_017008457.2:c.682-7983_682-7982del	XP_016863946.1:n.682-7983_682-7982del
XM_017008458.2:c.682-7983_682-7982del	XP_016863947.1:n.682-7983_682-7982del
XM_017008459.1:c.220-7983_220-7982del	XP_016863948.1:n.220-7983_220-7982del
XM_017008460.2:c.286-7983_286-7982del	XP_016863949.1:n.286-7983_286-7982del
XM_024454150.1:c.682-7983_682-7982del	XP_024309918.1:n.682-7983_682-7982del
XM_024454151.1:c.295-7983_295-7982del	XP_024309919.1:n.295-7983_295-7982del
XM_024454152.1:c.682-7983_682-7982del	XP_024309920.1:n.682-7983_682-7982del
XM_024454153.1:c.682-7983_682-7982del	XP_024309921.1:n.682-7983_682-7982del
XR_001741290.1:n.855-7983_855-7982del
XR_001741291.1:n.855-7983_855-7982del
XR_925341.3:n.859-7983_859-7982del
NM_020041.3:c.682-7983_682-7982del MANE Select	NP_064425.2:n.682-7983_682-7982del
NM_001001290.2:c.595-7983_595-7982del	NP_001001290.1:n.595-7983_595-7982del