Canonical Allele Identifier: CA360805980
Gene: SLC22A5 HGNC NCBI

Linked Data

dbSNP Id: rs1456314715

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132388925A>G , CM000667.2:g.132388925A>G GRCh38
NC_000005.9:g.131724617A>G , CM000667.1:g.131724617A>G GRCh37
NC_000005.8:g.131752516A>G NCBI36
NG_008982.1:g.24217A>G
NG_008982.2:g.24222A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.797A>G ENSP00000388838.2:p.Gln266Arg
ENST00000435065.7:c.1028A>G ENSP00000402760.2:p.Gln343Arg
ENST00000448810.6:c.956A>G ENSP00000401860.2:p.Gln319Arg
ENST00000685543.1:n.1097A>G
ENST00000686757.1:c.*120A>G ENSP00000510721.1:n.*120A>G
ENST00000687740.1:n.3641A>G
ENST00000688151.1:n.2266A>G
ENST00000689271.1:c.803A>G ENSP00000510797.1:p.Gln268Arg
ENST00000690900.1:c.*120A>G ENSP00000510703.1:n.*120A>G
ENST00000692212.1:n.900A>G
ENST00000692355.1:c.209A>G
ENST00000692413.1:c.938A>G ENSP00000509374.1:p.Gln313Arg
ENST00000692825.1:c.1024A>G ENSP00000509447.1:n.1024A>G
ENST00000693308.1:c.1004A>G ENSP00000509770.1:p.Gln335Arg
ENST00000693763.1:n.2116A>G
ENST00000245407.8:c.956A>G MANE Select ENSP00000245407.3:p.Gln319Arg
ENST00000245407.7:c.956A>G ENSP00000245407.3:p.Gln319Arg
ENST00000435065.6:c.1028A>G ENSP00000402760.2:p.Gln343Arg
ENST00000437841.6:c.*271A>G ENSP00000400553.1:n.*271A>G
ENST00000447841.5:c.15A>G
ENST00000448810.5:c.304A>G
ENST00000461013.5:n.8378A>G
ENST00000479605.5:n.59A>G
NM_001308122.1:c.1028A>G NP_001295051.1:p.Gln343Arg
NM_003060.3:c.956A>G NP_003051.1:p.Gln319Arg
XM_011543590.1:c.338A>G XP_011541892.1:p.Gln113Arg
XR_427718.1:n.1316A>G
XR_948290.1:n.1297A>G
XR_948291.1:n.1310A>G
XM_011543590.2:c.338A>G XP_011541892.1:p.Gln113Arg
XM_017009778.2:c.428A>G XP_016865267.1:p.Gln143Arg
XR_001742215.1:n.1297A>G
XR_001742216.1:n.1316A>G
XR_427718.2:n.1316A>G
XR_948290.2:n.1297A>G
XR_948291.2:n.1310A>G
NM_003060.4:c.956A>G MANE Select NP_003051.1:p.Gln319Arg
NM_001308122.2:c.1028A>G NP_001295051.1:p.Gln343Arg