Canonical Allele Identifier: CA1583146182
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132387047T= , CM000667.2:g.132387047T= GRCh38
NC_000005.9:g.131722739T= , CM000667.1:g.131722739T= GRCh37
NC_000005.8:g.131750638T= NCBI36
NG_008982.1:g.22339T=
NG_008982.2:g.22344T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.688T= ENSP00000388838.2:p.Trp230=
ENST00000435065.7:c.919T= ENSP00000402760.2:p.Trp307=
ENST00000448810.6:c.847T= ENSP00000401860.2:p.Trp283=
ENST00000686757.1:c.*11T= ENSP00000510721.1:n.*11T=
ENST00000687740.1:n.3532T=
ENST00000688151.1:n.2157T=
ENST00000689271.1:c.694T= ENSP00000510797.1:p.Trp232=
ENST00000690900.1:c.*11T= ENSP00000510703.1:n.*11T=
ENST00000692212.1:n.791T=
ENST00000692355.1:c.205-1874T=
ENST00000692413.1:c.844-15T= ENSP00000509374.1:n.844-15T=
ENST00000692825.1:c.915T= ENSP00000509447.1:n.915T=
ENST00000693308.1:c.895T= ENSP00000509770.1:p.Trp299=
ENST00000693763.1:n.2007T=
ENST00000245407.8:c.847T= MANE Select ENSP00000245407.3:p.Trp283=
ENST00000245407.7:c.847T= ENSP00000245407.3:p.Trp283=
ENST00000415928.5:c.616T= ENSP00000388838.1:p.Trp206=
ENST00000435065.6:c.919T= ENSP00000402760.2:p.Trp307=
ENST00000437841.6:c.*162T= ENSP00000400553.1:n.*162T=
ENST00000448810.5:c.195T=
ENST00000461013.5:n.8269T=
NM_001308122.1:c.919T= NP_001295051.1:p.Trp307=
NM_003060.3:c.847T= NP_003051.1:p.Trp283=
XM_011543590.1:c.229T= XP_011541892.1:p.Trp77=
XR_427718.1:n.1207T=
XR_948290.1:n.1188T=
XR_948291.1:n.1201T=
XM_011543590.2:c.229T= XP_011541892.1:p.Trp77=
XM_017009778.2:c.319T= XP_016865267.1:p.Trp107=
XR_001742215.1:n.1188T=
XR_001742216.1:n.1207T=
XR_427718.2:n.1207T=
XR_948290.2:n.1188T=
XR_948291.2:n.1201T=
NM_003060.4:c.847T= MANE Select NP_003051.1:p.Trp283=
NM_001308122.2:c.919T= NP_001295051.1:p.Trp307=