Canonical Allele Identifier: CA1583149914
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390722C= , CM000667.2:g.132390722C= GRCh38
NC_000005.9:g.131726414C= , CM000667.1:g.131726414C= GRCh37
NC_000005.8:g.131754313C= NCBI36
NG_008982.1:g.26014C=
NG_008982.2:g.26019C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.926C= ENSP00000388838.2:p.Ser309=
ENST00000435065.7:c.1157C= ENSP00000402760.2:p.Ser386=
ENST00000448810.6:c.1053-54C= ENSP00000401860.2:n.1053-54C=
ENST00000685543.1:n.1226C=
ENST00000686757.1:c.*249C= ENSP00000510721.1:n.*249C=
ENST00000687740.1:n.3770C=
ENST00000688151.1:n.2395C=
ENST00000689271.1:c.932C= ENSP00000510797.1:p.Ser311=
ENST00000690900.1:c.*249C= ENSP00000510703.1:n.*249C=
ENST00000692212.1:n.2697C=
ENST00000692355.1:c.338C=
ENST00000692413.1:c.1067C= ENSP00000509374.1:p.Ser356=
ENST00000692825.1:c.1153C= ENSP00000509447.1:n.1153C=
ENST00000693308.1:c.1133C= ENSP00000509770.1:p.Ser378=
ENST00000693763.1:n.2245C=
ENST00000245407.8:c.1085C= MANE Select ENSP00000245407.3:p.Ser362=
ENST00000245407.7:c.1085C= ENSP00000245407.3:p.Ser362=
ENST00000435065.6:c.1157C= ENSP00000402760.2:p.Ser386=
ENST00000447841.5:c.111+1701C=
ENST00000448810.5:c.401-54C=
ENST00000461013.5:n.8507C=
ENST00000475308.1:n.1763C=
ENST00000479605.5:n.188C=
NM_001308122.1:c.1157C= NP_001295051.1:p.Ser386=
NM_003060.3:c.1085C= NP_003051.1:p.Ser362=
XM_011543590.1:c.467C= XP_011541892.1:p.Ser156=
XR_427718.1:n.1445C=
XR_948290.1:n.1393+1701C=
XR_948291.1:n.1439C=
XM_011543590.2:c.467C= XP_011541892.1:p.Ser156=
XM_017009778.2:c.557C= XP_016865267.1:p.Ser186=
XR_001742215.1:n.1394-54C=
XR_001742216.1:n.1413-54C=
XR_427718.2:n.1445C=
XR_948290.2:n.1393+1701C=
XR_948291.2:n.1439C=
NM_003060.4:c.1085C= MANE Select NP_003051.1:p.Ser362=
NM_001308122.2:c.1157C= NP_001295051.1:p.Ser386=