Canonical Allele Identifier: CA1583144488
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393712G= , CM000667.2:g.132393712G= GRCh38
NC_000005.9:g.131729404G= , CM000667.1:g.131729404G= GRCh37
NC_000005.8:g.131757303G= NCBI36
NG_008982.1:g.29004G=
NG_008982.2:g.29009G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-473G= ENSP00000388838.2:n.1292-473G=
ENST00000435065.7:c.1559G= ENSP00000402760.2:p.Gly520=
ENST00000448810.6:c.*339G= ENSP00000401860.2:n.*339G=
ENST00000685543.1:n.1628G=
ENST00000686757.1:c.*651G= ENSP00000510721.1:n.*651G=
ENST00000686868.1:n.479G=
ENST00000687740.1:n.4172G=
ENST00000688151.1:n.2797G=
ENST00000689271.1:c.1334G= ENSP00000510797.1:p.Gly445=
ENST00000690900.1:c.*651G= ENSP00000510703.1:n.*651G=
ENST00000692212.1:n.4627G=
ENST00000692355.1:c.740G=
ENST00000692413.1:c.1469G= ENSP00000509374.1:p.Gly490=
ENST00000692825.1:c.1555G= ENSP00000509447.1:n.1555G=
ENST00000693308.1:c.1535G= ENSP00000509770.1:p.Gly512=
ENST00000693763.1:n.2647G=
ENST00000245407.8:c.1487G= MANE Select ENSP00000245407.3:p.Gly496=
ENST00000245407.7:c.1487G= ENSP00000245407.3:p.Gly496=
ENST00000435065.6:c.1559G= ENSP00000402760.2:p.Gly520=
ENST00000447841.5:c.331G=
ENST00000448810.5:c.749G=
ENST00000461013.5:n.8909G=
ENST00000475308.1:n.2165G=
NM_001308122.1:c.1559G= NP_001295051.1:p.Gly520=
NM_003060.3:c.1487G= NP_003051.1:p.Gly496=
XM_011543590.1:c.869G= XP_011541892.1:p.Gly290=
XR_948290.1:n.1613G=
XM_011543590.2:c.869G= XP_011541892.1:p.Gly290=
XM_017009778.2:c.959G= XP_016865267.1:p.Gly320=
XR_001742215.1:n.1742G=
XR_001742216.1:n.1761G=
XR_427718.2:n.1847G=
XR_948290.2:n.1613G=
XR_948291.2:n.1841G=
NM_003060.4:c.1487G= MANE Select NP_003051.1:p.Gly496=
NM_001308122.2:c.1559G= NP_001295051.1:p.Gly520=