Canonical Allele Identifier: CA1437785927
Gene: SLC2A9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.9980700C= , CM000666.2:g.9980700C= GRCh38
NC_000004.11:g.9982324C= , CM000666.1:g.9982324C= GRCh37
NC_000004.10:g.9591422C= NCBI36
NG_011540.1:g.64549G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264784.8:c.573G= MANE Select ENSP00000264784.3:p.Glu191=
ENST00000264784.7:c.573G= ENSP00000264784.3:p.Glu191=
ENST00000309065.7:c.486G= ENSP00000311383.3:p.Glu162=
ENST00000505104.5:n.607G=
ENST00000506583.5:c.486G= ENSP00000422209.1:p.Glu162=
ENST00000513129.1:c.486G= ENSP00000426800.1:p.Glu162=
NM_001001290.1:c.486G= NP_001001290.1:p.Glu162=
NM_020041.2:c.573G= NP_064425.2:p.Glu191=
XM_006713968.2:c.573G= XP_006714031.1:p.Glu191=
XM_006713969.2:c.486G= XP_006714032.1:p.Glu162=
XM_011513856.1:c.573G= XP_011512158.1:p.Glu191=
XM_011513857.1:c.486G= XP_011512159.1:p.Glu162=
XM_011513858.1:c.486G= XP_011512160.1:p.Glu162=
XM_011513859.1:c.573G= XP_011512161.1:p.Glu191=
XM_011513860.1:c.573G= XP_011512162.1:p.Glu191=
XM_011513861.1:c.573G= XP_011512163.1:p.Glu191=
XM_011513862.1:c.177G= XP_011512164.1:p.Glu59=
XM_011513863.1:c.177G= XP_011512165.1:p.Glu59=
XM_011513864.1:c.165G= XP_011512166.1:p.Glu55=
XM_011513865.1:c.573G= XP_011512167.1:p.Glu191=
XM_011513866.1:c.573G= XP_011512168.1:p.Glu191=
XM_011513867.1:c.15G= XP_011512169.1:p.Glu5=
XM_011513868.1:c.573G= XP_011512170.1:p.Glu191=
XR_925341.1:n.669G=
XM_006713968.4:c.573G= XP_006714031.1:p.Glu191=
XM_011513856.3:c.573G= XP_011512158.1:p.Glu191=
XM_011513859.3:c.573G= XP_011512161.1:p.Glu191=
XM_011513860.3:c.573G= XP_011512162.1:p.Glu191=
XM_011513861.3:c.573G= XP_011512163.1:p.Glu191=
XM_011513862.3:c.177G= XP_011512164.1:p.Glu59=
XM_011513864.2:c.165G= XP_011512166.1:p.Glu55=
XM_011513865.2:c.573G= XP_011512167.1:p.Glu191=
XM_011513866.2:c.573G= XP_011512168.1:p.Glu191=
XM_011513867.3:c.15G= XP_011512169.1:p.Glu5=
XM_011513868.2:c.573G= XP_011512170.1:p.Glu191=
XM_017008457.2:c.573G= XP_016863946.1:p.Glu191=
XM_017008458.2:c.573G= XP_016863947.1:p.Glu191=
XM_017008459.1:c.111G= XP_016863948.1:p.Glu37=
XM_017008460.2:c.177G= XP_016863949.1:p.Glu59=
XM_024454150.1:c.573G= XP_024309918.1:p.Glu191=
XM_024454151.1:c.186G= XP_024309919.1:p.Glu62=
XM_024454152.1:c.573G= XP_024309920.1:p.Glu191=
XM_024454153.1:c.573G= XP_024309921.1:p.Glu191=
XR_001741290.1:n.746G=
XR_001741291.1:n.746G=
XR_925341.3:n.750G=
NM_020041.3:c.573G= MANE Select NP_064425.2:p.Glu191=
NM_001001290.2:c.486G= NP_001001290.1:p.Glu162=