Canonical Allele Identifier: CA360805002
Gene: SLC22A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132385361T>A , CM000667.2:g.132385361T>A GRCh38
NC_000005.9:g.131721053T>A , CM000667.1:g.131721053T>A GRCh37
NC_000005.8:g.131748952T>A NCBI36
NG_008982.1:g.20653T>A
NG_008982.2:g.20658T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000415928.6:c.665+1047T>A ENSP00000388838.2:n.665+1047T>A
ENST00000435065.7:c.758T>A ENSP00000402760.2:p.Ile253Lys
ENST00000448810.6:c.686T>A ENSP00000401860.2:p.Ile229Lys
ENST00000686757.1:c.705T>A ENSP00000510721.1:p.Asn235Lys
ENST00000687740.1:n.1846T>A
ENST00000688151.1:n.1878T>A
ENST00000689271.1:c.671+1041T>A ENSP00000510797.1:n.671+1041T>A
ENST00000690900.1:c.672-15T>A ENSP00000510703.1:n.672-15T>A
ENST00000692212.1:n.512T>A
ENST00000692355.1:c.204+1060T>A
ENST00000692413.1:c.705T>A ENSP00000509374.1:p.Asn235Lys
ENST00000692825.1:c.754T>A ENSP00000509447.1:n.754T>A
ENST00000693308.1:c.699T>A ENSP00000509770.1:p.Asn233Lys
ENST00000693763.1:n.1846T>A
ENST00000245407.8:c.686T>A MANE Select ENSP00000245407.3:p.Ile229Lys
ENST00000245407.7:c.686T>A ENSP00000245407.3:p.Ile229Lys
ENST00000415928.5:c.455T>A ENSP00000388838.1:p.Ile152Lys
ENST00000435065.6:c.758T>A ENSP00000402760.2:p.Ile253Lys
ENST00000437841.6:c.*1T>A ENSP00000400553.1:n.*1T>A
ENST00000448810.5:c.34T>A
ENST00000461013.5:n.8108T>A
NM_001308122.1:c.758T>A NP_001295051.1:p.Ile253Lys
NM_003060.3:c.686T>A NP_003051.1:p.Ile229Lys
XM_011543590.1:c.68T>A XP_011541892.1:p.Ile23Lys
XR_427718.1:n.1046T>A
XR_948290.1:n.1027T>A
XR_948291.1:n.1040T>A
XM_011543590.2:c.68T>A XP_011541892.1:p.Ile23Lys
XM_017009778.2:c.158T>A XP_016865267.1:p.Ile53Lys
XR_001742215.1:n.1027T>A
XR_001742216.1:n.1046T>A
XR_427718.2:n.1046T>A
XR_948290.2:n.1027T>A
XR_948291.2:n.1040T>A
NM_003060.4:c.686T>A MANE Select NP_003051.1:p.Ile229Lys
NM_001308122.2:c.758T>A NP_001295051.1:p.Ile253Lys