Canonical Allele Identifier: CA2675200355
Gene: SLC22A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132385520del , CM000667.2:g.132385520del GRCh38
NC_000005.9:g.131721212del , CM000667.1:g.131721212del GRCh37
NC_000005.8:g.131749111del NCBI36
NG_008982.1:g.20812del
NG_008982.2:g.20817del

Transcript Alleles

HGVS Amino-acid change
ENST00000415928.6:c.665+1206del ENSP00000388838.2:n.665+1206del
ENST00000435065.7:c.896+21del ENSP00000402760.2:n.896+21del
ENST00000448810.6:c.824+21del ENSP00000401860.2:n.824+21del
ENST00000686757.1:c.843+21del ENSP00000510721.1:n.843+21del
ENST00000687740.1:n.2005del
ENST00000688151.1:n.2016+21del
ENST00000689271.1:c.671+1200del ENSP00000510797.1:n.671+1200del
ENST00000690900.1:c.795+21del ENSP00000510703.1:n.795+21del
ENST00000692212.1:n.650+21del
ENST00000692355.1:c.204+1219del
ENST00000692413.1:c.843+21del ENSP00000509374.1:n.843+21del
ENST00000692825.1:c.892+21del ENSP00000509447.1:n.892+21del
ENST00000693308.1:c.837+21del ENSP00000509770.1:n.837+21del
ENST00000693763.1:n.1984+21del
ENST00000245407.8:c.824+21del MANE Select ENSP00000245407.3:n.824+21del
ENST00000245407.7:c.824+21del ENSP00000245407.3:n.824+21del
ENST00000415928.5:c.593+21del ENSP00000388838.1:n.593+21del
ENST00000435065.6:c.896+21del ENSP00000402760.2:n.896+21del
ENST00000437841.6:c.*139+21del ENSP00000400553.1:n.*139+21del
ENST00000448810.5:c.172+21del
ENST00000461013.5:n.8246+21del
NM_001308122.1:c.896+21del NP_001295051.1:n.896+21del
NM_003060.3:c.824+21del NP_003051.1:n.824+21del
XM_011543590.1:c.206+21del XP_011541892.1:n.206+21del
XR_427718.1:n.1184+21del
XR_948290.1:n.1165+21del
XR_948291.1:n.1178+21del
XM_011543590.2:c.206+21del XP_011541892.1:n.206+21del
XM_017009778.2:c.296+21del XP_016865267.1:n.296+21del
XR_001742215.1:n.1165+21del
XR_001742216.1:n.1184+21del
XR_427718.2:n.1184+21del
XR_948290.2:n.1165+21del
XR_948291.2:n.1178+21del
NM_003060.4:c.824+21del MANE Select NP_003051.1:n.824+21del
NM_001308122.2:c.896+21del NP_001295051.1:n.896+21del