Canonical Allele Identifier: CA1583144576
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132385369A= , CM000667.2:g.132385369A= GRCh38
NC_000005.9:g.131721061A= , CM000667.1:g.131721061A= GRCh37
NC_000005.8:g.131748960A= NCBI36
NG_008982.1:g.20661A=
NG_008982.2:g.20666A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.665+1055A= ENSP00000388838.2:n.665+1055A=
ENST00000435065.7:c.766A= ENSP00000402760.2:p.Thr256=
ENST00000448810.6:c.694A= ENSP00000401860.2:p.Thr232=
ENST00000686757.1:c.713A= ENSP00000510721.1:p.Tyr238=
ENST00000687740.1:n.1854A=
ENST00000688151.1:n.1886A=
ENST00000689271.1:c.671+1049A= ENSP00000510797.1:n.671+1049A=
ENST00000690900.1:c.672-7A= ENSP00000510703.1:n.672-7A=
ENST00000692212.1:n.520A=
ENST00000692355.1:c.204+1068A=
ENST00000692413.1:c.713A= ENSP00000509374.1:p.Tyr238=
ENST00000692825.1:c.762A= ENSP00000509447.1:n.762A=
ENST00000693308.1:c.707A= ENSP00000509770.1:p.Tyr236=
ENST00000693763.1:n.1854A=
ENST00000245407.8:c.694A= MANE Select ENSP00000245407.3:p.Thr232=
ENST00000245407.7:c.694A= ENSP00000245407.3:p.Thr232=
ENST00000415928.5:c.463A= ENSP00000388838.1:p.Thr155=
ENST00000435065.6:c.766A= ENSP00000402760.2:p.Thr256=
ENST00000437841.6:c.*9A= ENSP00000400553.1:n.*9A=
ENST00000448810.5:c.42A=
ENST00000461013.5:n.8116A=
NM_001308122.1:c.766A= NP_001295051.1:p.Thr256=
NM_003060.3:c.694A= NP_003051.1:p.Thr232=
XM_011543590.1:c.76A= XP_011541892.1:p.Thr26=
XR_427718.1:n.1054A=
XR_948290.1:n.1035A=
XR_948291.1:n.1048A=
XM_011543590.2:c.76A= XP_011541892.1:p.Thr26=
XM_017009778.2:c.166A= XP_016865267.1:p.Thr56=
XR_001742215.1:n.1035A=
XR_001742216.1:n.1054A=
XR_427718.2:n.1054A=
XR_948290.2:n.1035A=
XR_948291.2:n.1048A=
NM_003060.4:c.694A= MANE Select NP_003051.1:p.Thr232=
NM_001308122.2:c.766A= NP_001295051.1:p.Thr256=