Canonical Allele Identifier: CA800758327

Gene: SLC2A9 SLC2A9-AS1

Linked Data

• dbSNP Id: rs1236126588
• gnomAD v3: 4-9992502-C-T
• gnomAD v4: 4-9992502-C-T
• MyVariant Identifiers: chr4:g.9994126C>T (hg19) ; chr4:g.9992502C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.9992502C>T , CM000666.2:g.9992502C>T	GRCh38
NC_000004.11:g.9994126C>T , CM000666.1:g.9994126C>T	GRCh37
NC_000004.10:g.9603224C>T	NCBI36
NG_011540.1:g.52747G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264784.8:c.410+4279G>A (SLC2A9) MANE Select	ENSP00000264784.3:n.410+4279G>A
ENST00000264784.7:c.410+4279G>A (SLC2A9)	ENSP00000264784.3:n.410+4279G>A
ENST00000309065.7:c.323+4279G>A (SLC2A9)	ENSP00000311383.3:n.323+4279G>A
ENST00000505104.5:n.444+4279G>A (SLC2A9)
ENST00000506583.5:c.323+4279G>A (SLC2A9)	ENSP00000422209.1:n.323+4279G>A
ENST00000506839.1:n.321-6709G>A (SLC2A9)
ENST00000513129.1:c.323+4279G>A (SLC2A9)	ENSP00000426800.1:n.323+4279G>A
NM_001001290.1:c.323+4279G>A (SLC2A9)	NP_001001290.1:n.323+4279G>A
NM_020041.2:c.410+4279G>A (SLC2A9)	NP_064425.2:n.410+4279G>A
XM_006713968.2:c.410+4279G>A (SLC2A9)	XP_006714031.1:n.410+4279G>A
XM_006713969.2:c.323+4279G>A (SLC2A9)	XP_006714032.1:n.323+4279G>A
XM_011513856.1:c.410+4279G>A (SLC2A9)	XP_011512158.1:n.410+4279G>A
XM_011513857.1:c.323+4279G>A (SLC2A9)	XP_011512159.1:n.323+4279G>A
XM_011513858.1:c.323+4279G>A (SLC2A9)	XP_011512160.1:n.323+4279G>A
XM_011513859.1:c.410+4279G>A (SLC2A9)	XP_011512161.1:n.410+4279G>A
XM_011513860.1:c.410+4279G>A (SLC2A9)	XP_011512162.1:n.410+4279G>A
XM_011513861.1:c.410+4279G>A (SLC2A9)	XP_011512163.1:n.410+4279G>A
XM_011513862.1:c.15-6709G>A (SLC2A9)	XP_011512164.1:n.15-6709G>A
XM_011513863.1:c.15-6709G>A (SLC2A9)	XP_011512165.1:n.15-6709G>A
XM_011513864.1:c.2+503G>A (SLC2A9)	XP_011512166.1:n.2+503G>A
XM_011513865.1:c.410+4279G>A (SLC2A9)	XP_011512167.1:n.410+4279G>A
XM_011513866.1:c.410+4279G>A (SLC2A9)	XP_011512168.1:n.410+4279G>A
XM_011513868.1:c.410+4279G>A (SLC2A9)	XP_011512170.1:n.410+4279G>A
XR_925341.1:n.506+4279G>A (SLC2A9)
XR_925367.1:n.164-753C>T (SLC2A9-AS1)
XM_006713968.4:c.410+4279G>A (SLC2A9)	XP_006714031.1:n.410+4279G>A
XM_011513856.3:c.410+4279G>A (SLC2A9)	XP_011512158.1:n.410+4279G>A
XM_011513859.3:c.410+4279G>A (SLC2A9)	XP_011512161.1:n.410+4279G>A
XM_011513860.3:c.410+4279G>A (SLC2A9)	XP_011512162.1:n.410+4279G>A
XM_011513861.3:c.410+4279G>A (SLC2A9)	XP_011512163.1:n.410+4279G>A
XM_011513862.3:c.15-6709G>A (SLC2A9)	XP_011512164.1:n.15-6709G>A
XM_011513864.2:c.2+503G>A (SLC2A9)	XP_011512166.1:n.2+503G>A
XM_011513865.2:c.410+4279G>A (SLC2A9)	XP_011512167.1:n.410+4279G>A
XM_011513866.2:c.410+4279G>A (SLC2A9)	XP_011512168.1:n.410+4279G>A
XM_011513868.2:c.410+4279G>A (SLC2A9)	XP_011512170.1:n.410+4279G>A
XM_017008457.2:c.410+4279G>A (SLC2A9)	XP_016863946.1:n.410+4279G>A
XM_017008458.2:c.410+4279G>A (SLC2A9)	XP_016863947.1:n.410+4279G>A
XM_017008459.1:c.-53+606G>A (SLC2A9)	XP_016863948.1:n.-53+606G>A
XM_017008460.2:c.15-6709G>A (SLC2A9)	XP_016863949.1:n.15-6709G>A
XM_024454150.1:c.410+4279G>A (SLC2A9)	XP_024309918.1:n.410+4279G>A
XM_024454151.1:c.23+4279G>A (SLC2A9)	XP_024309919.1:n.23+4279G>A
XM_024454152.1:c.410+4279G>A (SLC2A9)	XP_024309920.1:n.410+4279G>A
XM_024454153.1:c.410+4279G>A (SLC2A9)	XP_024309921.1:n.410+4279G>A
XR_001741290.1:n.583+4279G>A (SLC2A9)
XR_001741291.1:n.583+4279G>A (SLC2A9)
XR_001741589.1:n.311-753C>T (SLC2A9-AS1)
XR_925341.3:n.587+4279G>A (SLC2A9)
NM_020041.3:c.410+4279G>A (SLC2A9) MANE Select	NP_064425.2:n.410+4279G>A
NM_001001290.2:c.323+4279G>A (SLC2A9)	NP_001001290.1:n.323+4279G>A