Canonical Allele Identifier: CA1583144479
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393711G= , CM000667.2:g.132393711G= GRCh38
NC_000005.9:g.131729403G= , CM000667.1:g.131729403G= GRCh37
NC_000005.8:g.131757302G= NCBI36
NG_008982.1:g.29003G=
NG_008982.2:g.29008G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-474G= ENSP00000388838.2:n.1292-474G=
ENST00000435065.7:c.1558G= ENSP00000402760.2:p.Gly520=
ENST00000448810.6:c.*338G= ENSP00000401860.2:n.*338G=
ENST00000685543.1:n.1627G=
ENST00000686757.1:c.*650G= ENSP00000510721.1:n.*650G=
ENST00000686868.1:n.478G=
ENST00000687740.1:n.4171G=
ENST00000688151.1:n.2796G=
ENST00000689271.1:c.1333G= ENSP00000510797.1:p.Gly445=
ENST00000690900.1:c.*650G= ENSP00000510703.1:n.*650G=
ENST00000692212.1:n.4626G=
ENST00000692355.1:c.739G=
ENST00000692413.1:c.1468G= ENSP00000509374.1:p.Gly490=
ENST00000692825.1:c.1554G= ENSP00000509447.1:n.1554G=
ENST00000693308.1:c.1534G= ENSP00000509770.1:p.Gly512=
ENST00000693763.1:n.2646G=
ENST00000245407.8:c.1486G= MANE Select ENSP00000245407.3:p.Gly496=
ENST00000245407.7:c.1486G= ENSP00000245407.3:p.Gly496=
ENST00000435065.6:c.1558G= ENSP00000402760.2:p.Gly520=
ENST00000447841.5:c.330G=
ENST00000448810.5:c.748G=
ENST00000461013.5:n.8908G=
ENST00000475308.1:n.2164G=
NM_001308122.1:c.1558G= NP_001295051.1:p.Gly520=
NM_003060.3:c.1486G= NP_003051.1:p.Gly496=
XM_011543590.1:c.868G= XP_011541892.1:p.Gly290=
XR_948290.1:n.1612G=
XM_011543590.2:c.868G= XP_011541892.1:p.Gly290=
XM_017009778.2:c.958G= XP_016865267.1:p.Gly320=
XR_001742215.1:n.1741G=
XR_001742216.1:n.1760G=
XR_427718.2:n.1846G=
XR_948290.2:n.1612G=
XR_948291.2:n.1840G=
NM_003060.4:c.1486G= MANE Select NP_003051.1:p.Gly496=
NM_001308122.2:c.1558G= NP_001295051.1:p.Gly520=