Canonical Allele Identifier: CA1583150193
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390850A= , CM000667.2:g.132390850A= GRCh38
NC_000005.9:g.131726542A= , CM000667.1:g.131726542A= GRCh37
NC_000005.8:g.131754441A= NCBI36
NG_008982.1:g.26142A=
NG_008982.2:g.26147A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1054A= ENSP00000388838.2:p.Thr352=
ENST00000435065.7:c.1285A= ENSP00000402760.2:p.Thr429=
ENST00000448810.6:c.*65A= ENSP00000401860.2:n.*65A=
ENST00000685543.1:n.1354A=
ENST00000686757.1:c.*377A= ENSP00000510721.1:n.*377A=
ENST00000687740.1:n.3898A=
ENST00000688151.1:n.2523A=
ENST00000689271.1:c.1060A= ENSP00000510797.1:p.Thr354=
ENST00000690900.1:c.*377A= ENSP00000510703.1:n.*377A=
ENST00000692212.1:n.2825A=
ENST00000692355.1:c.466A=
ENST00000692413.1:c.1195A= ENSP00000509374.1:p.Thr399=
ENST00000692825.1:c.1281A= ENSP00000509447.1:n.1281A=
ENST00000693308.1:c.1261A= ENSP00000509770.1:p.Thr421=
ENST00000693763.1:n.2373A=
ENST00000245407.8:c.1213A= MANE Select ENSP00000245407.3:p.Thr405=
ENST00000245407.7:c.1213A= ENSP00000245407.3:p.Thr405=
ENST00000435065.6:c.1285A= ENSP00000402760.2:p.Thr429=
ENST00000447841.5:c.112-1583A=
ENST00000448810.5:c.475A=
ENST00000461013.5:n.8635A=
ENST00000475308.1:n.1891A=
ENST00000479605.5:n.316A=
NM_001308122.1:c.1285A= NP_001295051.1:p.Thr429=
NM_003060.3:c.1213A= NP_003051.1:p.Thr405=
XM_011543590.1:c.595A= XP_011541892.1:p.Thr199=
XR_427718.1:n.1573A=
XR_948290.1:n.1394-1583A=
XR_948291.1:n.1567A=
XM_011543590.2:c.595A= XP_011541892.1:p.Thr199=
XM_017009778.2:c.685A= XP_016865267.1:p.Thr229=
XR_001742215.1:n.1468A=
XR_001742216.1:n.1487A=
XR_427718.2:n.1573A=
XR_948290.2:n.1394-1583A=
XR_948291.2:n.1567A=
NM_003060.4:c.1213A= MANE Select NP_003051.1:p.Thr405=
NM_001308122.2:c.1285A= NP_001295051.1:p.Thr429=