Canonical Allele Identifier: CA1583150068
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390798T= , CM000667.2:g.132390798T= GRCh38
NC_000005.9:g.131726490T= , CM000667.1:g.131726490T= GRCh37
NC_000005.8:g.131754389T= NCBI36
NG_008982.1:g.26090T=
NG_008982.2:g.26095T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1002T= ENSP00000388838.2:p.Tyr334=
ENST00000435065.7:c.1233T= ENSP00000402760.2:p.Tyr411=
ENST00000448810.6:c.*13T= ENSP00000401860.2:n.*13T=
ENST00000685543.1:n.1302T=
ENST00000686757.1:c.*325T= ENSP00000510721.1:n.*325T=
ENST00000687740.1:n.3846T=
ENST00000688151.1:n.2471T=
ENST00000689271.1:c.1008T= ENSP00000510797.1:p.Tyr336=
ENST00000690900.1:c.*325T= ENSP00000510703.1:n.*325T=
ENST00000692212.1:n.2773T=
ENST00000692355.1:c.414T=
ENST00000692413.1:c.1143T= ENSP00000509374.1:p.Tyr381=
ENST00000692825.1:c.1229T= ENSP00000509447.1:n.1229T=
ENST00000693308.1:c.1209T= ENSP00000509770.1:p.Tyr403=
ENST00000693763.1:n.2321T=
ENST00000245407.8:c.1161T= MANE Select ENSP00000245407.3:p.Tyr387=
ENST00000245407.7:c.1161T= ENSP00000245407.3:p.Tyr387=
ENST00000435065.6:c.1233T= ENSP00000402760.2:p.Tyr411=
ENST00000447841.5:c.112-1635T=
ENST00000448810.5:c.423T=
ENST00000461013.5:n.8583T=
ENST00000475308.1:n.1839T=
ENST00000479605.5:n.264T=
NM_001308122.1:c.1233T= NP_001295051.1:p.Tyr411=
NM_003060.3:c.1161T= NP_003051.1:p.Tyr387=
XM_011543590.1:c.543T= XP_011541892.1:p.Tyr181=
XR_427718.1:n.1521T=
XR_948290.1:n.1394-1635T=
XR_948291.1:n.1515T=
XM_011543590.2:c.543T= XP_011541892.1:p.Tyr181=
XM_017009778.2:c.633T= XP_016865267.1:p.Tyr211=
XR_001742215.1:n.1416T=
XR_001742216.1:n.1435T=
XR_427718.2:n.1521T=
XR_948290.2:n.1394-1635T=
XR_948291.2:n.1515T=
NM_003060.4:c.1161T= MANE Select NP_003051.1:p.Tyr387=
NM_001308122.2:c.1233T= NP_001295051.1:p.Tyr411=