Canonical Allele Identifier: CA15341236
Gene: SLC2A9 HGNC NCBI

Linked Data

dbSNP Id: rs4580649

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.9946837G>A , CM000666.2:g.9946837G>A GRCh38
NC_000004.11:g.9948461G>A , CM000666.1:g.9948461G>A GRCh37
NC_000004.10:g.9557559G>A NCBI36
NG_011540.1:g.98412C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264784.8:c.682-4792C>T MANE Select ENSP00000264784.3:n.682-4792C>T
ENST00000264784.7:c.682-4792C>T ENSP00000264784.3:n.682-4792C>T
ENST00000309065.7:c.595-4792C>T ENSP00000311383.3:n.595-4792C>T
ENST00000505104.5:n.716-4792C>T
ENST00000506583.5:c.595-4792C>T ENSP00000422209.1:n.595-4792C>T
NM_001001290.1:c.595-4792C>T NP_001001290.1:n.595-4792C>T
NM_020041.2:c.682-4792C>T NP_064425.2:n.682-4792C>T
XM_006713968.2:c.682-4792C>T XP_006714031.1:n.682-4792C>T
XM_006713969.2:c.595-4792C>T XP_006714032.1:n.595-4792C>T
XM_011513856.1:c.682-4792C>T XP_011512158.1:n.682-4792C>T
XM_011513857.1:c.595-4792C>T XP_011512159.1:n.595-4792C>T
XM_011513858.1:c.595-4792C>T XP_011512160.1:n.595-4792C>T
XM_011513859.1:c.682-4792C>T XP_011512161.1:n.682-4792C>T
XM_011513860.1:c.682-4792C>T XP_011512162.1:n.682-4792C>T
XM_011513861.1:c.682-4792C>T XP_011512163.1:n.682-4792C>T
XM_011513862.1:c.286-4792C>T XP_011512164.1:n.286-4792C>T
XM_011513863.1:c.286-4792C>T XP_011512165.1:n.286-4792C>T
XM_011513864.1:c.274-4792C>T XP_011512166.1:n.274-4792C>T
XM_011513865.1:c.682-4792C>T XP_011512167.1:n.682-4792C>T
XM_011513866.1:c.682-4792C>T XP_011512168.1:n.682-4792C>T
XM_011513867.1:c.124-4792C>T XP_011512169.1:n.124-4792C>T
XM_011513868.1:c.682-4792C>T XP_011512170.1:n.682-4792C>T
XR_925341.1:n.778-4792C>T
XM_006713968.4:c.682-4792C>T XP_006714031.1:n.682-4792C>T
XM_011513856.3:c.682-4792C>T XP_011512158.1:n.682-4792C>T
XM_011513859.3:c.682-4792C>T XP_011512161.1:n.682-4792C>T
XM_011513860.3:c.682-4792C>T XP_011512162.1:n.682-4792C>T
XM_011513861.3:c.682-4792C>T XP_011512163.1:n.682-4792C>T
XM_011513862.3:c.286-4792C>T XP_011512164.1:n.286-4792C>T
XM_011513864.2:c.274-4792C>T XP_011512166.1:n.274-4792C>T
XM_011513865.2:c.682-4792C>T XP_011512167.1:n.682-4792C>T
XM_011513866.2:c.682-4792C>T XP_011512168.1:n.682-4792C>T
XM_011513867.3:c.124-4792C>T XP_011512169.1:n.124-4792C>T
XM_011513868.2:c.682-4792C>T XP_011512170.1:n.682-4792C>T
XM_017008457.2:c.682-4792C>T XP_016863946.1:n.682-4792C>T
XM_017008458.2:c.682-4792C>T XP_016863947.1:n.682-4792C>T
XM_017008459.1:c.220-4792C>T XP_016863948.1:n.220-4792C>T
XM_017008460.2:c.286-4792C>T XP_016863949.1:n.286-4792C>T
XM_024454150.1:c.682-4792C>T XP_024309918.1:n.682-4792C>T
XM_024454151.1:c.295-4792C>T XP_024309919.1:n.295-4792C>T
XM_024454152.1:c.682-4792C>T XP_024309920.1:n.682-4792C>T
XM_024454153.1:c.682-4792C>T XP_024309921.1:n.682-4792C>T
XR_001741290.1:n.855-4792C>T
XR_001741291.1:n.855-4792C>T
XR_925341.3:n.859-4792C>T
NM_020041.3:c.682-4792C>T MANE Select NP_064425.2:n.682-4792C>T
NM_001001290.2:c.595-4792C>T NP_001001290.1:n.595-4792C>T