Canonical Allele Identifier: CA1583149993
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390761A= , CM000667.2:g.132390761A= GRCh38
NC_000005.9:g.131726453A= , CM000667.1:g.131726453A= GRCh37
NC_000005.8:g.131754352A= NCBI36
NG_008982.1:g.26053A=
NG_008982.2:g.26058A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.965A= ENSP00000388838.2:p.Asn322=
ENST00000435065.7:c.1196A= ENSP00000402760.2:p.Asn399=
ENST00000448810.6:c.1053-15A= ENSP00000401860.2:n.1053-15A=
ENST00000685543.1:n.1265A=
ENST00000686757.1:c.*288A= ENSP00000510721.1:n.*288A=
ENST00000687740.1:n.3809A=
ENST00000688151.1:n.2434A=
ENST00000689271.1:c.971A= ENSP00000510797.1:p.Asn324=
ENST00000690900.1:c.*288A= ENSP00000510703.1:n.*288A=
ENST00000692212.1:n.2736A=
ENST00000692355.1:c.377A=
ENST00000692413.1:c.1106A= ENSP00000509374.1:p.Asn369=
ENST00000692825.1:c.1192A= ENSP00000509447.1:n.1192A=
ENST00000693308.1:c.1172A= ENSP00000509770.1:p.Asn391=
ENST00000693763.1:n.2284A=
ENST00000245407.8:c.1124A= MANE Select ENSP00000245407.3:p.Asn375=
ENST00000245407.7:c.1124A= ENSP00000245407.3:p.Asn375=
ENST00000435065.6:c.1196A= ENSP00000402760.2:p.Asn399=
ENST00000447841.5:c.112-1672A=
ENST00000448810.5:c.401-15A=
ENST00000461013.5:n.8546A=
ENST00000475308.1:n.1802A=
ENST00000479605.5:n.227A=
NM_001308122.1:c.1196A= NP_001295051.1:p.Asn399=
NM_003060.3:c.1124A= NP_003051.1:p.Asn375=
XM_011543590.1:c.506A= XP_011541892.1:p.Asn169=
XR_427718.1:n.1484A=
XR_948290.1:n.1394-1672A=
XR_948291.1:n.1478A=
XM_011543590.2:c.506A= XP_011541892.1:p.Asn169=
XM_017009778.2:c.596A= XP_016865267.1:p.Asn199=
XR_001742215.1:n.1394-15A=
XR_001742216.1:n.1413-15A=
XR_427718.2:n.1484A=
XR_948290.2:n.1394-1672A=
XR_948291.2:n.1478A=
NM_003060.4:c.1124A= MANE Select NP_003051.1:p.Asn375=
NM_001308122.2:c.1196A= NP_001295051.1:p.Asn399=