Canonical Allele Identifier: CA1583150296
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390895G= , CM000667.2:g.132390895G= GRCh38
NC_000005.9:g.131726587G= , CM000667.1:g.131726587G= GRCh37
NC_000005.8:g.131754486G= NCBI36
NG_008982.1:g.26187G=
NG_008982.2:g.26192G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1099G= ENSP00000388838.2:p.Val367=
ENST00000435065.7:c.1330G= ENSP00000402760.2:p.Val444=
ENST00000448810.6:c.*110G= ENSP00000401860.2:n.*110G=
ENST00000685543.1:n.1399G=
ENST00000686757.1:c.*422G= ENSP00000510721.1:n.*422G=
ENST00000687740.1:n.3943G=
ENST00000688151.1:n.2568G=
ENST00000689271.1:c.1105G= ENSP00000510797.1:p.Val369=
ENST00000690900.1:c.*422G= ENSP00000510703.1:n.*422G=
ENST00000692212.1:n.2870G=
ENST00000692355.1:c.511G=
ENST00000692413.1:c.1240G= ENSP00000509374.1:p.Val414=
ENST00000692825.1:c.1326G= ENSP00000509447.1:n.1326G=
ENST00000693308.1:c.1306G= ENSP00000509770.1:p.Val436=
ENST00000693763.1:n.2418G=
ENST00000245407.8:c.1258G= MANE Select ENSP00000245407.3:p.Val420=
ENST00000245407.7:c.1258G= ENSP00000245407.3:p.Val420=
ENST00000435065.6:c.1330G= ENSP00000402760.2:p.Val444=
ENST00000447841.5:c.112-1538G=
ENST00000448810.5:c.520G=
ENST00000461013.5:n.8680G=
ENST00000475308.1:n.1936G=
ENST00000479605.5:n.361G=
NM_001308122.1:c.1330G= NP_001295051.1:p.Val444=
NM_003060.3:c.1258G= NP_003051.1:p.Val420=
XM_011543590.1:c.640G= XP_011541892.1:p.Val214=
XR_427718.1:n.1618G=
XR_948290.1:n.1394-1538G=
XR_948291.1:n.1612G=
XM_011543590.2:c.640G= XP_011541892.1:p.Val214=
XM_017009778.2:c.730G= XP_016865267.1:p.Val244=
XR_001742215.1:n.1513G=
XR_001742216.1:n.1532G=
XR_427718.2:n.1618G=
XR_948290.2:n.1394-1538G=
XR_948291.2:n.1612G=
NM_003060.4:c.1258G= MANE Select NP_003051.1:p.Val420=
NM_001308122.2:c.1330G= NP_001295051.1:p.Val444=