Canonical Allele Identifier: CA1583144526
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132385306C= , CM000667.2:g.132385306C= GRCh38
NC_000005.9:g.131720998C= , CM000667.1:g.131720998C= GRCh37
NC_000005.8:g.131748897C= NCBI36
NG_008982.1:g.20598C=
NG_008982.2:g.20603C=

Transcript Alleles

HGVS Amino-acid change
ENST00000415928.6:c.665+992C= ENSP00000388838.2:n.665+992C=
ENST00000435065.7:c.725-22C= ENSP00000402760.2:n.725-22C=
ENST00000448810.6:c.653-22C= ENSP00000401860.2:n.653-22C=
ENST00000686757.1:c.672-22C= ENSP00000510721.1:n.672-22C=
ENST00000687740.1:n.1791C=
ENST00000688151.1:n.1845-22C=
ENST00000689271.1:c.671+986C= ENSP00000510797.1:n.671+986C=
ENST00000690900.1:c.672-70C= ENSP00000510703.1:n.672-70C=
ENST00000692212.1:n.457C=
ENST00000692355.1:c.204+1005C=
ENST00000692413.1:c.672-22C= ENSP00000509374.1:n.672-22C=
ENST00000692825.1:c.721-22C= ENSP00000509447.1:n.721-22C=
ENST00000693308.1:c.666-22C= ENSP00000509770.1:n.666-22C=
ENST00000693763.1:n.1791C=
ENST00000245407.8:c.653-22C= MANE Select ENSP00000245407.3:n.653-22C=
ENST00000245407.7:c.653-22C= ENSP00000245407.3:n.653-22C=
ENST00000415928.5:c.422-22C= ENSP00000388838.1:n.422-22C=
ENST00000435065.6:c.725-22C= ENSP00000402760.2:n.725-22C=
ENST00000437841.6:c.394-22C= ENSP00000400553.1:n.394-22C=
ENST00000461013.5:n.8075-22C=
NM_001308122.1:c.725-22C= NP_001295051.1:n.725-22C=
NM_003060.3:c.653-22C= NP_003051.1:n.653-22C=
XM_011543590.1:c.35-22C= XP_011541892.1:n.35-22C=
XR_427718.1:n.1013-22C=
XR_948290.1:n.994-22C=
XR_948291.1:n.1007-22C=
XM_011543590.2:c.35-22C= XP_011541892.1:n.35-22C=
XM_017009778.2:c.125-22C= XP_016865267.1:n.125-22C=
XR_001742215.1:n.994-22C=
XR_001742216.1:n.1013-22C=
XR_427718.2:n.1013-22C=
XR_948290.2:n.994-22C=
XR_948291.2:n.1007-22C=
NM_003060.4:c.653-22C= MANE Select NP_003051.1:n.653-22C=
NM_001308122.2:c.725-22C= NP_001295051.1:n.725-22C=