Canonical Allele Identifier: CA356400842

Gene: SLC2A9

Linked Data

• MyVariant Identifiers: chr4:g.9922063C>G (hg19) ; chr4:g.9920439C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.9920439C>G , CM000666.2:g.9920439C>G	GRCh38
NC_000004.11:g.9922063C>G , CM000666.1:g.9922063C>G	GRCh37
NC_000004.10:g.9531161C>G	NCBI36
NG_011540.1:g.124810G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264784.8:c.948G>C MANE Select	ENSP00000264784.3:p.Gln316His
ENST00000264784.7:c.948G>C	ENSP00000264784.3:p.Gln316His
ENST00000309065.7:c.861G>C	ENSP00000311383.3:p.Gln287His
ENST00000505104.5:n.982G>C
ENST00000506583.5:c.861G>C	ENSP00000422209.1:p.Gln287His
NM_001001290.1:c.861G>C	NP_001001290.1:p.Gln287His
NM_020041.2:c.948G>C	NP_064425.2:p.Gln316His
XM_006713968.2:c.948G>C	XP_006714031.1:p.Gln316His
XM_006713969.2:c.861G>C	XP_006714032.1:p.Gln287His
XM_011513856.1:c.948G>C	XP_011512158.1:p.Gln316His
XM_011513857.1:c.861G>C	XP_011512159.1:p.Gln287His
XM_011513858.1:c.861G>C	XP_011512160.1:p.Gln287His
XM_011513859.1:c.948G>C	XP_011512161.1:p.Gln316His
XM_011513860.1:c.948G>C	XP_011512162.1:p.Gln316His
XM_011513861.1:c.948G>C	XP_011512163.1:p.Gln316His
XM_011513862.1:c.552G>C	XP_011512164.1:p.Gln184His
XM_011513863.1:c.552G>C	XP_011512165.1:p.Gln184His
XM_011513864.1:c.540G>C	XP_011512166.1:p.Gln180His
XM_011513865.1:c.948G>C	XP_011512167.1:p.Gln316His
XM_011513866.1:c.948G>C	XP_011512168.1:p.Gln316His
XM_011513867.1:c.390G>C	XP_011512169.1:p.Gln130His
XM_011513868.1:c.948G>C	XP_011512170.1:p.Gln316His
XR_925341.1:n.1044G>C
XM_006713968.4:c.948G>C	XP_006714031.1:p.Gln316His
XM_011513856.3:c.948G>C	XP_011512158.1:p.Gln316His
XM_011513859.3:c.948G>C	XP_011512161.1:p.Gln316His
XM_011513860.3:c.948G>C	XP_011512162.1:p.Gln316His
XM_011513861.3:c.948G>C	XP_011512163.1:p.Gln316His
XM_011513862.3:c.552G>C	XP_011512164.1:p.Gln184His
XM_011513864.2:c.540G>C	XP_011512166.1:p.Gln180His
XM_011513865.2:c.948G>C	XP_011512167.1:p.Gln316His
XM_011513866.2:c.948G>C	XP_011512168.1:p.Gln316His
XM_011513867.3:c.390G>C	XP_011512169.1:p.Gln130His
XM_011513868.2:c.948G>C	XP_011512170.1:p.Gln316His
XM_017008457.2:c.948G>C	XP_016863946.1:p.Gln316His
XM_017008458.2:c.948G>C	XP_016863947.1:p.Gln316His
XM_017008459.1:c.486G>C	XP_016863948.1:p.Gln162His
XM_017008460.2:c.552G>C	XP_016863949.1:p.Gln184His
XM_024454150.1:c.948G>C	XP_024309918.1:p.Gln316His
XM_024454151.1:c.561G>C	XP_024309919.1:p.Gln187His
XM_024454152.1:c.948G>C	XP_024309920.1:p.Gln316His
XM_024454153.1:c.948G>C	XP_024309921.1:p.Gln316His
XR_001741290.1:n.1121G>C
XR_001741291.1:n.1121G>C
XR_925341.3:n.1125G>C
NM_020041.3:c.948G>C MANE Select	NP_064425.2:p.Gln316His
NM_001001290.2:c.861G>C	NP_001001290.1:p.Gln287His