Canonical Allele Identifier: CA356400885

Gene: SLC2A9

Linked Data

• MyVariant Identifiers: chr4:g.9922085C>G (hg19) ; chr4:g.9920461C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.9920461C>G , CM000666.2:g.9920461C>G	GRCh38
NC_000004.11:g.9922085C>G , CM000666.1:g.9922085C>G	GRCh37
NC_000004.10:g.9531183C>G	NCBI36
NG_011540.1:g.124788G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264784.8:c.926G>C MANE Select	ENSP00000264784.3:p.Arg309Thr
ENST00000264784.7:c.926G>C	ENSP00000264784.3:p.Arg309Thr
ENST00000309065.7:c.839G>C	ENSP00000311383.3:p.Arg280Thr
ENST00000505104.5:n.960G>C
ENST00000506583.5:c.839G>C	ENSP00000422209.1:p.Arg280Thr
NM_001001290.1:c.839G>C	NP_001001290.1:p.Arg280Thr
NM_020041.2:c.926G>C	NP_064425.2:p.Arg309Thr
XM_006713968.2:c.926G>C	XP_006714031.1:p.Arg309Thr
XM_006713969.2:c.839G>C	XP_006714032.1:p.Arg280Thr
XM_011513856.1:c.926G>C	XP_011512158.1:p.Arg309Thr
XM_011513857.1:c.839G>C	XP_011512159.1:p.Arg280Thr
XM_011513858.1:c.839G>C	XP_011512160.1:p.Arg280Thr
XM_011513859.1:c.926G>C	XP_011512161.1:p.Arg309Thr
XM_011513860.1:c.926G>C	XP_011512162.1:p.Arg309Thr
XM_011513861.1:c.926G>C	XP_011512163.1:p.Arg309Thr
XM_011513862.1:c.530G>C	XP_011512164.1:p.Arg177Thr
XM_011513863.1:c.530G>C	XP_011512165.1:p.Arg177Thr
XM_011513864.1:c.518G>C	XP_011512166.1:p.Arg173Thr
XM_011513865.1:c.926G>C	XP_011512167.1:p.Arg309Thr
XM_011513866.1:c.926G>C	XP_011512168.1:p.Arg309Thr
XM_011513867.1:c.368G>C	XP_011512169.1:p.Arg123Thr
XM_011513868.1:c.926G>C	XP_011512170.1:p.Arg309Thr
XR_925341.1:n.1022G>C
XM_006713968.4:c.926G>C	XP_006714031.1:p.Arg309Thr
XM_011513856.3:c.926G>C	XP_011512158.1:p.Arg309Thr
XM_011513859.3:c.926G>C	XP_011512161.1:p.Arg309Thr
XM_011513860.3:c.926G>C	XP_011512162.1:p.Arg309Thr
XM_011513861.3:c.926G>C	XP_011512163.1:p.Arg309Thr
XM_011513862.3:c.530G>C	XP_011512164.1:p.Arg177Thr
XM_011513864.2:c.518G>C	XP_011512166.1:p.Arg173Thr
XM_011513865.2:c.926G>C	XP_011512167.1:p.Arg309Thr
XM_011513866.2:c.926G>C	XP_011512168.1:p.Arg309Thr
XM_011513867.3:c.368G>C	XP_011512169.1:p.Arg123Thr
XM_011513868.2:c.926G>C	XP_011512170.1:p.Arg309Thr
XM_017008457.2:c.926G>C	XP_016863946.1:p.Arg309Thr
XM_017008458.2:c.926G>C	XP_016863947.1:p.Arg309Thr
XM_017008459.1:c.464G>C	XP_016863948.1:p.Arg155Thr
XM_017008460.2:c.530G>C	XP_016863949.1:p.Arg177Thr
XM_024454150.1:c.926G>C	XP_024309918.1:p.Arg309Thr
XM_024454151.1:c.539G>C	XP_024309919.1:p.Arg180Thr
XM_024454152.1:c.926G>C	XP_024309920.1:p.Arg309Thr
XM_024454153.1:c.926G>C	XP_024309921.1:p.Arg309Thr
XR_001741290.1:n.1099G>C
XR_001741291.1:n.1099G>C
XR_925341.3:n.1103G>C
NM_020041.3:c.926G>C MANE Select	NP_064425.2:p.Arg309Thr
NM_001001290.2:c.839G>C	NP_001001290.1:p.Arg280Thr