Canonical Allele Identifier: CA1583150052
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390786A= , CM000667.2:g.132390786A= GRCh38
NC_000005.9:g.131726478A= , CM000667.1:g.131726478A= GRCh37
NC_000005.8:g.131754377A= NCBI36
NG_008982.1:g.26078A=
NG_008982.2:g.26083A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.990A= ENSP00000388838.2:p.Glu330=
ENST00000435065.7:c.1221A= ENSP00000402760.2:p.Glu407=
ENST00000448810.6:c.*1A= ENSP00000401860.2:n.*1A=
ENST00000685543.1:n.1290A=
ENST00000686757.1:c.*313A= ENSP00000510721.1:n.*313A=
ENST00000687740.1:n.3834A=
ENST00000688151.1:n.2459A=
ENST00000689271.1:c.996A= ENSP00000510797.1:p.Glu332=
ENST00000690900.1:c.*313A= ENSP00000510703.1:n.*313A=
ENST00000692212.1:n.2761A=
ENST00000692355.1:c.402A=
ENST00000692413.1:c.1131A= ENSP00000509374.1:p.Glu377=
ENST00000692825.1:c.1217A= ENSP00000509447.1:n.1217A=
ENST00000693308.1:c.1197A= ENSP00000509770.1:p.Glu399=
ENST00000693763.1:n.2309A=
ENST00000245407.8:c.1149A= MANE Select ENSP00000245407.3:p.Glu383=
ENST00000245407.7:c.1149A= ENSP00000245407.3:p.Glu383=
ENST00000435065.6:c.1221A= ENSP00000402760.2:p.Glu407=
ENST00000447841.5:c.112-1647A=
ENST00000448810.5:c.411A=
ENST00000461013.5:n.8571A=
ENST00000475308.1:n.1827A=
ENST00000479605.5:n.252A=
NM_001308122.1:c.1221A= NP_001295051.1:p.Glu407=
NM_003060.3:c.1149A= NP_003051.1:p.Glu383=
XM_011543590.1:c.531A= XP_011541892.1:p.Glu177=
XR_427718.1:n.1509A=
XR_948290.1:n.1394-1647A=
XR_948291.1:n.1503A=
XM_011543590.2:c.531A= XP_011541892.1:p.Glu177=
XM_017009778.2:c.621A= XP_016865267.1:p.Glu207=
XR_001742215.1:n.1404A=
XR_001742216.1:n.1423A=
XR_427718.2:n.1509A=
XR_948290.2:n.1394-1647A=
XR_948291.2:n.1503A=
NM_003060.4:c.1149A= MANE Select NP_003051.1:p.Glu383=
NM_001308122.2:c.1221A= NP_001295051.1:p.Glu407=