Canonical Allele Identifier: CA1583144446
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393692C= , CM000667.2:g.132393692C= GRCh38
NC_000005.9:g.131729384C= , CM000667.1:g.131729384C= GRCh37
NC_000005.8:g.131757283C= NCBI36
NG_008982.1:g.28984C=
NG_008982.2:g.28989C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-493C= ENSP00000388838.2:n.1292-493C=
ENST00000435065.7:c.1539C= ENSP00000402760.2:p.Phe513=
ENST00000448810.6:c.*319C= ENSP00000401860.2:n.*319C=
ENST00000685543.1:n.1608C=
ENST00000686757.1:c.*631C= ENSP00000510721.1:n.*631C=
ENST00000686868.1:n.459C=
ENST00000687740.1:n.4152C=
ENST00000688151.1:n.2777C=
ENST00000689271.1:c.1314C= ENSP00000510797.1:p.Phe438=
ENST00000690900.1:c.*631C= ENSP00000510703.1:n.*631C=
ENST00000692212.1:n.4607C=
ENST00000692355.1:c.720C=
ENST00000692413.1:c.1449C= ENSP00000509374.1:p.Phe483=
ENST00000692825.1:c.1535C= ENSP00000509447.1:n.1535C=
ENST00000693308.1:c.1515C= ENSP00000509770.1:p.Phe505=
ENST00000693763.1:n.2627C=
ENST00000245407.8:c.1467C= MANE Select ENSP00000245407.3:p.Phe489=
ENST00000245407.7:c.1467C= ENSP00000245407.3:p.Phe489=
ENST00000435065.6:c.1539C= ENSP00000402760.2:p.Phe513=
ENST00000447841.5:c.311C=
ENST00000448810.5:c.729C=
ENST00000461013.5:n.8889C=
ENST00000475308.1:n.2145C=
NM_001308122.1:c.1539C= NP_001295051.1:p.Phe513=
NM_003060.3:c.1467C= NP_003051.1:p.Phe489=
XM_011543590.1:c.849C= XP_011541892.1:p.Phe283=
XR_948290.1:n.1593C=
XM_011543590.2:c.849C= XP_011541892.1:p.Phe283=
XM_017009778.2:c.939C= XP_016865267.1:p.Phe313=
XR_001742215.1:n.1722C=
XR_001742216.1:n.1741C=
XR_427718.2:n.1827C=
XR_948290.2:n.1593C=
XR_948291.2:n.1821C=
NM_003060.4:c.1467C= MANE Select NP_003051.1:p.Phe489=
NM_001308122.2:c.1539C= NP_001295051.1:p.Phe513=