Canonical Allele Identifier: CA356400801

Gene: SLC2A9

Linked Data

• MyVariant Identifiers: chr4:g.9922043G>C (hg19) ; chr4:g.9920419G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.9920419G>C , CM000666.2:g.9920419G>C	GRCh38
NC_000004.11:g.9922043G>C , CM000666.1:g.9922043G>C	GRCh37
NC_000004.10:g.9531141G>C	NCBI36
NG_011540.1:g.124830C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264784.8:c.968C>G MANE Select	ENSP00000264784.3:p.Thr323Ser
ENST00000264784.7:c.968C>G	ENSP00000264784.3:p.Thr323Ser
ENST00000309065.7:c.881C>G	ENSP00000311383.3:p.Thr294Ser
ENST00000505104.5:n.1002C>G
ENST00000506583.5:c.881C>G	ENSP00000422209.1:p.Thr294Ser
NM_001001290.1:c.881C>G	NP_001001290.1:p.Thr294Ser
NM_020041.2:c.968C>G	NP_064425.2:p.Thr323Ser
XM_006713968.2:c.968C>G	XP_006714031.1:p.Thr323Ser
XM_006713969.2:c.881C>G	XP_006714032.1:p.Thr294Ser
XM_011513856.1:c.968C>G	XP_011512158.1:p.Thr323Ser
XM_011513857.1:c.881C>G	XP_011512159.1:p.Thr294Ser
XM_011513858.1:c.881C>G	XP_011512160.1:p.Thr294Ser
XM_011513859.1:c.968C>G	XP_011512161.1:p.Thr323Ser
XM_011513860.1:c.968C>G	XP_011512162.1:p.Thr323Ser
XM_011513861.1:c.968C>G	XP_011512163.1:p.Thr323Ser
XM_011513862.1:c.572C>G	XP_011512164.1:p.Thr191Ser
XM_011513863.1:c.572C>G	XP_011512165.1:p.Thr191Ser
XM_011513864.1:c.560C>G	XP_011512166.1:p.Thr187Ser
XM_011513865.1:c.968C>G	XP_011512167.1:p.Thr323Ser
XM_011513866.1:c.968C>G	XP_011512168.1:p.Thr323Ser
XM_011513867.1:c.410C>G	XP_011512169.1:p.Thr137Ser
XM_011513868.1:c.968C>G	XP_011512170.1:p.Thr323Ser
XR_925341.1:n.1064C>G
XM_006713968.4:c.968C>G	XP_006714031.1:p.Thr323Ser
XM_011513856.3:c.968C>G	XP_011512158.1:p.Thr323Ser
XM_011513859.3:c.968C>G	XP_011512161.1:p.Thr323Ser
XM_011513860.3:c.968C>G	XP_011512162.1:p.Thr323Ser
XM_011513861.3:c.968C>G	XP_011512163.1:p.Thr323Ser
XM_011513862.3:c.572C>G	XP_011512164.1:p.Thr191Ser
XM_011513864.2:c.560C>G	XP_011512166.1:p.Thr187Ser
XM_011513865.2:c.968C>G	XP_011512167.1:p.Thr323Ser
XM_011513866.2:c.968C>G	XP_011512168.1:p.Thr323Ser
XM_011513867.3:c.410C>G	XP_011512169.1:p.Thr137Ser
XM_011513868.2:c.968C>G	XP_011512170.1:p.Thr323Ser
XM_017008457.2:c.968C>G	XP_016863946.1:p.Thr323Ser
XM_017008458.2:c.968C>G	XP_016863947.1:p.Thr323Ser
XM_017008459.1:c.506C>G	XP_016863948.1:p.Thr169Ser
XM_017008460.2:c.572C>G	XP_016863949.1:p.Thr191Ser
XM_024454150.1:c.968C>G	XP_024309918.1:p.Thr323Ser
XM_024454151.1:c.581C>G	XP_024309919.1:p.Thr194Ser
XM_024454152.1:c.968C>G	XP_024309920.1:p.Thr323Ser
XM_024454153.1:c.968C>G	XP_024309921.1:p.Thr323Ser
XR_001741290.1:n.1141C>G
XR_001741291.1:n.1141C>G
XR_925341.3:n.1145C>G
NM_020041.3:c.968C>G MANE Select	NP_064425.2:p.Thr323Ser
NM_001001290.2:c.881C>G	NP_001001290.1:p.Thr294Ser