Canonical Allele Identifier: CA1583150113
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390814C= , CM000667.2:g.132390814C= GRCh38
NC_000005.9:g.131726506C= , CM000667.1:g.131726506C= GRCh37
NC_000005.8:g.131754405C= NCBI36
NG_008982.1:g.26106C=
NG_008982.2:g.26111C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1018C= ENSP00000388838.2:p.Leu340=
ENST00000435065.7:c.1249C= ENSP00000402760.2:p.Leu417=
ENST00000448810.6:c.*29C= ENSP00000401860.2:n.*29C=
ENST00000685543.1:n.1318C=
ENST00000686757.1:c.*341C= ENSP00000510721.1:n.*341C=
ENST00000687740.1:n.3862C=
ENST00000688151.1:n.2487C=
ENST00000689271.1:c.1024C= ENSP00000510797.1:p.Leu342=
ENST00000690900.1:c.*341C= ENSP00000510703.1:n.*341C=
ENST00000692212.1:n.2789C=
ENST00000692355.1:c.430C=
ENST00000692413.1:c.1159C= ENSP00000509374.1:p.Leu387=
ENST00000692825.1:c.1245C= ENSP00000509447.1:n.1245C=
ENST00000693308.1:c.1225C= ENSP00000509770.1:p.Leu409=
ENST00000693763.1:n.2337C=
ENST00000245407.8:c.1177C= MANE Select ENSP00000245407.3:p.Leu393=
ENST00000245407.7:c.1177C= ENSP00000245407.3:p.Leu393=
ENST00000435065.6:c.1249C= ENSP00000402760.2:p.Leu417=
ENST00000447841.5:c.112-1619C=
ENST00000448810.5:c.439C=
ENST00000461013.5:n.8599C=
ENST00000475308.1:n.1855C=
ENST00000479605.5:n.280C=
NM_001308122.1:c.1249C= NP_001295051.1:p.Leu417=
NM_003060.3:c.1177C= NP_003051.1:p.Leu393=
XM_011543590.1:c.559C= XP_011541892.1:p.Leu187=
XR_427718.1:n.1537C=
XR_948290.1:n.1394-1619C=
XR_948291.1:n.1531C=
XM_011543590.2:c.559C= XP_011541892.1:p.Leu187=
XM_017009778.2:c.649C= XP_016865267.1:p.Leu217=
XR_001742215.1:n.1432C=
XR_001742216.1:n.1451C=
XR_427718.2:n.1537C=
XR_948290.2:n.1394-1619C=
XR_948291.2:n.1531C=
NM_003060.4:c.1177C= MANE Select NP_003051.1:p.Leu393=
NM_001308122.2:c.1249C= NP_001295051.1:p.Leu417=