Canonical Allele Identifier: CA11679472
Gene: SLC2A9 HGNC NCBI

Linked Data

dbSNP Id: rs3775948

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.9993558G>C , CM000666.2:g.9993558G>C GRCh38
NC_000004.11:g.9995182G>C , CM000666.1:g.9995182G>C GRCh37
NC_000004.10:g.9604280G>C NCBI36
NG_011540.1:g.51691C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000264784.8:c.410+3223C>G MANE Select ENSP00000264784.3:p.=
ENST00000264784.7:c.410+3223C>G ENSP00000264784.3:p.=
ENST00000309065.7:c.323+3223C>G ENSP00000311383.3:p.=
ENST00000505104.5:n.444+3223C>G
ENST00000506583.5:c.323+3223C>G ENSP00000422209.1:p.=
ENST00000506839.1:n.321-7765C>G
ENST00000513129.1:c.323+3223C>G ENSP00000426800.1:p.=
NM_001001290.1:c.323+3223C>G NP_001001290.1:p.=
NM_020041.2:c.410+3223C>G NP_064425.2:p.=
XM_006713968.2:c.410+3223C>G XP_006714031.1:p.=
XM_006713969.2:c.323+3223C>G XP_006714032.1:p.=
XM_011513856.1:c.410+3223C>G XP_011512158.1:p.=
XM_011513857.1:c.323+3223C>G XP_011512159.1:p.=
XM_011513858.1:c.323+3223C>G XP_011512160.1:p.=
XM_011513859.1:c.410+3223C>G XP_011512161.1:p.=
XM_011513860.1:c.410+3223C>G XP_011512162.1:p.=
XM_011513861.1:c.410+3223C>G XP_011512163.1:p.=
XM_011513862.1:c.15-7765C>G XP_011512164.1:p.=
XM_011513863.1:c.15-7765C>G XP_011512165.1:p.=
XM_011513865.1:c.410+3223C>G XP_011512167.1:p.=
XM_011513866.1:c.410+3223C>G XP_011512168.1:p.=
XM_011513868.1:c.410+3223C>G XP_011512170.1:p.=
XR_925341.1:n.506+3223C>G
XR_925367.1:n.283+184G>C
XM_006713968.4:c.410+3223C>G XP_006714031.1:p.=
XM_011513856.3:c.410+3223C>G XP_011512158.1:p.=
XM_011513859.3:c.410+3223C>G XP_011512161.1:p.=
XM_011513860.3:c.410+3223C>G XP_011512162.1:p.=
XM_011513861.3:c.410+3223C>G XP_011512163.1:p.=
XM_011513862.3:c.15-7765C>G XP_011512164.1:p.=
XM_011513865.2:c.410+3223C>G XP_011512167.1:p.=
XM_011513866.2:c.410+3223C>G XP_011512168.1:p.=
XM_011513868.2:c.410+3223C>G XP_011512170.1:p.=
XM_017008457.2:c.410+3223C>G XP_016863946.1:p.=
XM_017008458.2:c.410+3223C>G XP_016863947.1:p.=
XM_017008460.2:c.15-7765C>G XP_016863949.1:p.=
XM_024454150.1:c.410+3223C>G XP_024309918.1:p.=
XM_024454151.1:c.23+3223C>G XP_024309919.1:p.=
XM_024454152.1:c.410+3223C>G XP_024309920.1:p.=
XM_024454153.1:c.410+3223C>G XP_024309921.1:p.=
XR_001741290.1:n.583+3223C>G
XR_001741291.1:n.583+3223C>G
XR_001741589.1:n.430+184G>C
XR_001741590.1:n.80+184G>C
XR_001741591.1:n.80+184G>C
XR_001741592.1:n.80+184G>C
XR_925341.3:n.587+3223C>G
NM_020041.3:c.410+3223C>G MANE Select NP_064425.2:p.=
NM_001001290.2:c.323+3223C>G NP_001001290.1:p.=