Canonical Allele Identifier: CA360807547
Gene: SLC22A5 HGNC NCBI

Linked Data

dbSNP Id: rs1409873849

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390749A>G , CM000667.2:g.132390749A>G GRCh38
NC_000005.9:g.131726441A>G , CM000667.1:g.131726441A>G GRCh37
NC_000005.8:g.131754340A>G NCBI36
NG_008982.1:g.26041A>G
NG_008982.2:g.26046A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000415928.6:c.953A>G ENSP00000388838.2:p.Asp318Gly
ENST00000435065.7:c.1184A>G ENSP00000402760.2:p.Asp395Gly
ENST00000448810.6:c.1053-27A>G ENSP00000401860.2:n.1053-27A>G
ENST00000685543.1:n.1253A>G
ENST00000686757.1:c.*276A>G ENSP00000510721.1:n.*276A>G
ENST00000687740.1:n.3797A>G
ENST00000688151.1:n.2422A>G
ENST00000689271.1:c.959A>G ENSP00000510797.1:p.Asp320Gly
ENST00000690900.1:c.*276A>G ENSP00000510703.1:n.*276A>G
ENST00000692212.1:n.2724A>G
ENST00000692355.1:c.365A>G
ENST00000692413.1:c.1094A>G ENSP00000509374.1:p.Asp365Gly
ENST00000692825.1:c.1180A>G ENSP00000509447.1:n.1180A>G
ENST00000693308.1:c.1160A>G ENSP00000509770.1:p.Asp387Gly
ENST00000693763.1:n.2272A>G
ENST00000245407.8:c.1112A>G MANE Select ENSP00000245407.3:p.Asp371Gly
ENST00000245407.7:c.1112A>G ENSP00000245407.3:p.Asp371Gly
ENST00000435065.6:c.1184A>G ENSP00000402760.2:p.Asp395Gly
ENST00000447841.5:c.112-1684A>G
ENST00000448810.5:c.401-27A>G
ENST00000461013.5:n.8534A>G
ENST00000475308.1:n.1790A>G
ENST00000479605.5:n.215A>G
NM_001308122.1:c.1184A>G NP_001295051.1:p.Asp395Gly
NM_003060.3:c.1112A>G NP_003051.1:p.Asp371Gly
XM_011543590.1:c.494A>G XP_011541892.1:p.Asp165Gly
XR_427718.1:n.1472A>G
XR_948290.1:n.1394-1684A>G
XR_948291.1:n.1466A>G
XM_011543590.2:c.494A>G XP_011541892.1:p.Asp165Gly
XM_017009778.2:c.584A>G XP_016865267.1:p.Asp195Gly
XR_001742215.1:n.1394-27A>G
XR_001742216.1:n.1413-27A>G
XR_427718.2:n.1472A>G
XR_948290.2:n.1394-1684A>G
XR_948291.2:n.1466A>G
NM_003060.4:c.1112A>G MANE Select NP_003051.1:p.Asp371Gly
NM_001308122.2:c.1184A>G NP_001295051.1:p.Asp395Gly