Canonical Allele Identifier: CA1583150132
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390822A= , CM000667.2:g.132390822A= GRCh38
NC_000005.9:g.131726514A= , CM000667.1:g.131726514A= GRCh37
NC_000005.8:g.131754413A= NCBI36
NG_008982.1:g.26114A=
NG_008982.2:g.26119A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1026A= ENSP00000388838.2:p.Gln342=
ENST00000435065.7:c.1257A= ENSP00000402760.2:p.Gln419=
ENST00000448810.6:c.*37A= ENSP00000401860.2:n.*37A=
ENST00000685543.1:n.1326A=
ENST00000686757.1:c.*349A= ENSP00000510721.1:n.*349A=
ENST00000687740.1:n.3870A=
ENST00000688151.1:n.2495A=
ENST00000689271.1:c.1032A= ENSP00000510797.1:p.Gln344=
ENST00000690900.1:c.*349A= ENSP00000510703.1:n.*349A=
ENST00000692212.1:n.2797A=
ENST00000692355.1:c.438A=
ENST00000692413.1:c.1167A= ENSP00000509374.1:p.Gln389=
ENST00000692825.1:c.1253A= ENSP00000509447.1:n.1253A=
ENST00000693308.1:c.1233A= ENSP00000509770.1:p.Gln411=
ENST00000693763.1:n.2345A=
ENST00000245407.8:c.1185A= MANE Select ENSP00000245407.3:p.Gln395=
ENST00000245407.7:c.1185A= ENSP00000245407.3:p.Gln395=
ENST00000435065.6:c.1257A= ENSP00000402760.2:p.Gln419=
ENST00000447841.5:c.112-1611A=
ENST00000448810.5:c.447A=
ENST00000461013.5:n.8607A=
ENST00000475308.1:n.1863A=
ENST00000479605.5:n.288A=
NM_001308122.1:c.1257A= NP_001295051.1:p.Gln419=
NM_003060.3:c.1185A= NP_003051.1:p.Gln395=
XM_011543590.1:c.567A= XP_011541892.1:p.Gln189=
XR_427718.1:n.1545A=
XR_948290.1:n.1394-1611A=
XR_948291.1:n.1539A=
XM_011543590.2:c.567A= XP_011541892.1:p.Gln189=
XM_017009778.2:c.657A= XP_016865267.1:p.Gln219=
XR_001742215.1:n.1440A=
XR_001742216.1:n.1459A=
XR_427718.2:n.1545A=
XR_948290.2:n.1394-1611A=
XR_948291.2:n.1539A=
NM_003060.4:c.1185A= MANE Select NP_003051.1:p.Gln395=
NM_001308122.2:c.1257A= NP_001295051.1:p.Gln419=