Canonical Allele Identifier: CA1583144472
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132385200C= , CM000667.2:g.132385200C= GRCh38
NC_000005.9:g.131720892C= , CM000667.1:g.131720892C= GRCh37
NC_000005.8:g.131748791C= NCBI36
NG_008982.1:g.20492C=
NG_008982.2:g.20497C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.665+886C= ENSP00000388838.2:n.665+886C=
ENST00000435065.7:c.725-128C= ENSP00000402760.2:n.725-128C=
ENST00000448810.6:c.653-128C= ENSP00000401860.2:n.653-128C=
ENST00000686757.1:c.672-128C= ENSP00000510721.1:n.672-128C=
ENST00000687740.1:n.1685C=
ENST00000688151.1:n.1845-128C=
ENST00000689271.1:c.671+880C= ENSP00000510797.1:n.671+880C=
ENST00000690900.1:c.672-176C= ENSP00000510703.1:n.672-176C=
ENST00000692212.1:n.351C=
ENST00000692355.1:c.204+899C=
ENST00000692413.1:c.672-128C= ENSP00000509374.1:n.672-128C=
ENST00000692825.1:c.721-128C= ENSP00000509447.1:n.721-128C=
ENST00000693308.1:c.666-128C= ENSP00000509770.1:n.666-128C=
ENST00000693763.1:n.1685C=
ENST00000245407.8:c.653-128C= MANE Select ENSP00000245407.3:n.653-128C=
ENST00000245407.7:c.653-128C= ENSP00000245407.3:n.653-128C=
ENST00000415928.5:c.422-128C= ENSP00000388838.1:n.422-128C=
ENST00000435065.6:c.725-128C= ENSP00000402760.2:n.725-128C=
ENST00000437841.6:c.394-128C= ENSP00000400553.1:n.394-128C=
ENST00000461013.5:n.8075-128C=
NM_001308122.1:c.725-128C= NP_001295051.1:n.725-128C=
NM_003060.3:c.653-128C= NP_003051.1:n.653-128C=
XM_011543590.1:c.35-128C= XP_011541892.1:n.35-128C=
XR_427718.1:n.1013-128C=
XR_948290.1:n.994-128C=
XR_948291.1:n.1007-128C=
XM_011543590.2:c.35-128C= XP_011541892.1:n.35-128C=
XM_017009778.2:c.125-128C= XP_016865267.1:n.125-128C=
XR_001742215.1:n.994-128C=
XR_001742216.1:n.1013-128C=
XR_427718.2:n.1013-128C=
XR_948290.2:n.994-128C=
XR_948291.2:n.1007-128C=
NM_003060.4:c.653-128C= MANE Select NP_003051.1:n.653-128C=
NM_001308122.2:c.725-128C= NP_001295051.1:n.725-128C=