Canonical Allele Identifier: CA2675199831
Gene: SLC22A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393917del , CM000667.2:g.132393917del GRCh38
NC_000005.9:g.131729609del , CM000667.1:g.131729609del GRCh37
NC_000005.8:g.131757508del NCBI36
NG_008982.1:g.29209del
NG_008982.2:g.29214del

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-268del ENSP00000388838.2:n.1292-268del
ENST00000435065.7:c.1658+106del ENSP00000402760.2:n.1658+106del
ENST00000448810.6:c.*438+106del ENSP00000401860.2:n.*438+106del
ENST00000685543.1:n.1727+106del
ENST00000686757.1:c.*750+106del ENSP00000510721.1:n.*750+106del
ENST00000686868.1:n.578+106del
ENST00000687740.1:n.4271+106del
ENST00000688151.1:n.2896+106del
ENST00000689271.1:c.1433+106del ENSP00000510797.1:n.1433+106del
ENST00000690900.1:c.*750+106del ENSP00000510703.1:n.*750+106del
ENST00000692212.1:n.4726+106del
ENST00000692355.1:c.839+106del
ENST00000692413.1:c.1568+106del ENSP00000509374.1:n.1568+106del
ENST00000692825.1:c.1654+106del ENSP00000509447.1:n.1654+106del
ENST00000693308.1:c.1634+106del ENSP00000509770.1:n.1634+106del
ENST00000693763.1:n.2746+106del
ENST00000245407.8:c.1586+106del MANE Select ENSP00000245407.3:n.1586+106del
ENST00000245407.7:c.1586+106del ENSP00000245407.3:n.1586+106del
ENST00000435065.6:c.1658+106del ENSP00000402760.2:n.1658+106del
ENST00000447841.5:c.430+106del
ENST00000461013.5:n.9008+106del
ENST00000475308.1:n.2264+106del
NM_001308122.1:c.1658+106del NP_001295051.1:n.1658+106del
NM_003060.3:c.1586+106del NP_003051.1:n.1586+106del
XM_011543590.1:c.968+106del XP_011541892.1:n.968+106del
XR_948290.1:n.1712+106del
XM_011543590.2:c.968+106del XP_011541892.1:n.968+106del
XM_017009778.2:c.1058+106del XP_016865267.1:n.1058+106del
XR_001742215.1:n.1841+106del
XR_001742216.1:n.1860+106del
XR_427718.2:n.1946+106del
XR_948290.2:n.1712+106del
XR_948291.2:n.1940+106del
NM_003060.4:c.1586+106del MANE Select NP_003051.1:n.1586+106del
NM_001308122.2:c.1658+106del NP_001295051.1:n.1658+106del