Canonical Allele Identifier: CA2675200396
Gene: SLC22A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132385528del , CM000667.2:g.132385528del GRCh38
NC_000005.9:g.131721220del , CM000667.1:g.131721220del GRCh37
NC_000005.8:g.131749119del NCBI36
NG_008982.1:g.20820del
NG_008982.2:g.20825del

Transcript Alleles

HGVS Amino-acid change
ENST00000415928.6:c.665+1214del ENSP00000388838.2:n.665+1214del
ENST00000435065.7:c.896+29del ENSP00000402760.2:n.896+29del
ENST00000448810.6:c.824+29del ENSP00000401860.2:n.824+29del
ENST00000686757.1:c.843+29del ENSP00000510721.1:n.843+29del
ENST00000687740.1:n.2013del
ENST00000688151.1:n.2016+29del
ENST00000689271.1:c.671+1208del ENSP00000510797.1:n.671+1208del
ENST00000690900.1:c.795+29del ENSP00000510703.1:n.795+29del
ENST00000692212.1:n.650+29del
ENST00000692355.1:c.204+1227del
ENST00000692413.1:c.843+29del ENSP00000509374.1:n.843+29del
ENST00000692825.1:c.892+29del ENSP00000509447.1:n.892+29del
ENST00000693308.1:c.837+29del ENSP00000509770.1:n.837+29del
ENST00000693763.1:n.1984+29del
ENST00000245407.8:c.824+29del MANE Select ENSP00000245407.3:n.824+29del
ENST00000245407.7:c.824+29del ENSP00000245407.3:n.824+29del
ENST00000415928.5:c.593+29del ENSP00000388838.1:n.593+29del
ENST00000435065.6:c.896+29del ENSP00000402760.2:n.896+29del
ENST00000437841.6:c.*139+29del ENSP00000400553.1:n.*139+29del
ENST00000448810.5:c.172+29del
ENST00000461013.5:n.8246+29del
NM_001308122.1:c.896+29del NP_001295051.1:n.896+29del
NM_003060.3:c.824+29del NP_003051.1:n.824+29del
XM_011543590.1:c.206+29del XP_011541892.1:n.206+29del
XR_427718.1:n.1184+29del
XR_948290.1:n.1165+29del
XR_948291.1:n.1178+29del
XM_011543590.2:c.206+29del XP_011541892.1:n.206+29del
XM_017009778.2:c.296+29del XP_016865267.1:n.296+29del
XR_001742215.1:n.1165+29del
XR_001742216.1:n.1184+29del
XR_427718.2:n.1184+29del
XR_948290.2:n.1165+29del
XR_948291.2:n.1178+29del
NM_003060.4:c.824+29del MANE Select NP_003051.1:n.824+29del
NM_001308122.2:c.896+29del NP_001295051.1:n.896+29del