Canonical Allele Identifier: CA1583150293
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390892C= , CM000667.2:g.132390892C= GRCh38
NC_000005.9:g.131726584C= , CM000667.1:g.131726584C= GRCh37
NC_000005.8:g.131754483C= NCBI36
NG_008982.1:g.26184C=
NG_008982.2:g.26189C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1096C= ENSP00000388838.2:p.Leu366=
ENST00000435065.7:c.1327C= ENSP00000402760.2:p.Leu443=
ENST00000448810.6:c.*107C= ENSP00000401860.2:n.*107C=
ENST00000685543.1:n.1396C=
ENST00000686757.1:c.*419C= ENSP00000510721.1:n.*419C=
ENST00000687740.1:n.3940C=
ENST00000688151.1:n.2565C=
ENST00000689271.1:c.1102C= ENSP00000510797.1:p.Leu368=
ENST00000690900.1:c.*419C= ENSP00000510703.1:n.*419C=
ENST00000692212.1:n.2867C=
ENST00000692355.1:c.508C=
ENST00000692413.1:c.1237C= ENSP00000509374.1:p.Leu413=
ENST00000692825.1:c.1323C= ENSP00000509447.1:n.1323C=
ENST00000693308.1:c.1303C= ENSP00000509770.1:p.Leu435=
ENST00000693763.1:n.2415C=
ENST00000245407.8:c.1255C= MANE Select ENSP00000245407.3:p.Leu419=
ENST00000245407.7:c.1255C= ENSP00000245407.3:p.Leu419=
ENST00000435065.6:c.1327C= ENSP00000402760.2:p.Leu443=
ENST00000447841.5:c.112-1541C=
ENST00000448810.5:c.517C=
ENST00000461013.5:n.8677C=
ENST00000475308.1:n.1933C=
ENST00000479605.5:n.358C=
NM_001308122.1:c.1327C= NP_001295051.1:p.Leu443=
NM_003060.3:c.1255C= NP_003051.1:p.Leu419=
XM_011543590.1:c.637C= XP_011541892.1:p.Leu213=
XR_427718.1:n.1615C=
XR_948290.1:n.1394-1541C=
XR_948291.1:n.1609C=
XM_011543590.2:c.637C= XP_011541892.1:p.Leu213=
XM_017009778.2:c.727C= XP_016865267.1:p.Leu243=
XR_001742215.1:n.1510C=
XR_001742216.1:n.1529C=
XR_427718.2:n.1615C=
XR_948290.2:n.1394-1541C=
XR_948291.2:n.1609C=
NM_003060.4:c.1255C= MANE Select NP_003051.1:p.Leu419=
NM_001308122.2:c.1327C= NP_001295051.1:p.Leu443=