Canonical Allele Identifier: CA1583144434
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393687C= , CM000667.2:g.132393687C= GRCh38
NC_000005.9:g.131729379C= , CM000667.1:g.131729379C= GRCh37
NC_000005.8:g.131757278C= NCBI36
NG_008982.1:g.28979C=
NG_008982.2:g.28984C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-498C= ENSP00000388838.2:n.1292-498C=
ENST00000435065.7:c.1534C= ENSP00000402760.2:p.Arg512=
ENST00000448810.6:c.*314C= ENSP00000401860.2:n.*314C=
ENST00000685543.1:n.1603C=
ENST00000686757.1:c.*626C= ENSP00000510721.1:n.*626C=
ENST00000686868.1:n.454C=
ENST00000687740.1:n.4147C=
ENST00000688151.1:n.2772C=
ENST00000689271.1:c.1309C= ENSP00000510797.1:p.Arg437=
ENST00000690900.1:c.*626C= ENSP00000510703.1:n.*626C=
ENST00000692212.1:n.4602C=
ENST00000692355.1:c.715C=
ENST00000692413.1:c.1444C= ENSP00000509374.1:p.Arg482=
ENST00000692825.1:c.1530C= ENSP00000509447.1:n.1530C=
ENST00000693308.1:c.1510C= ENSP00000509770.1:p.Arg504=
ENST00000693763.1:n.2622C=
ENST00000245407.8:c.1462C= MANE Select ENSP00000245407.3:p.Arg488=
ENST00000245407.7:c.1462C= ENSP00000245407.3:p.Arg488=
ENST00000435065.6:c.1534C= ENSP00000402760.2:p.Arg512=
ENST00000447841.5:c.306C=
ENST00000448810.5:c.724C=
ENST00000461013.5:n.8884C=
ENST00000475308.1:n.2140C=
NM_001308122.1:c.1534C= NP_001295051.1:p.Arg512=
NM_003060.3:c.1462C= NP_003051.1:p.Arg488=
XM_011543590.1:c.844C= XP_011541892.1:p.Arg282=
XR_948290.1:n.1588C=
XM_011543590.2:c.844C= XP_011541892.1:p.Arg282=
XM_017009778.2:c.934C= XP_016865267.1:p.Arg312=
XR_001742215.1:n.1717C=
XR_001742216.1:n.1736C=
XR_427718.2:n.1822C=
XR_948290.2:n.1588C=
XR_948291.2:n.1816C=
NM_003060.4:c.1462C= MANE Select NP_003051.1:p.Arg488=
NM_001308122.2:c.1534C= NP_001295051.1:p.Arg512=