Canonical Allele Identifier: CA2675199397
Gene: SLC22A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393602del , CM000667.2:g.132393602del GRCh38
NC_000005.9:g.131729294del , CM000667.1:g.131729294del GRCh37
NC_000005.8:g.131757193del NCBI36
NG_008982.1:g.28894del
NG_008982.2:g.28899del

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-583del ENSP00000388838.2:n.1292-583del
ENST00000435065.7:c.1523-74del ENSP00000402760.2:n.1523-74del
ENST00000448810.6:c.*303-74del ENSP00000401860.2:n.*303-74del
ENST00000685543.1:n.1592-74del
ENST00000686757.1:c.*615-74del ENSP00000510721.1:n.*615-74del
ENST00000686868.1:n.369del
ENST00000687740.1:n.4136-74del
ENST00000688151.1:n.2761-74del
ENST00000689271.1:c.1298-74del ENSP00000510797.1:n.1298-74del
ENST00000690900.1:c.*615-74del ENSP00000510703.1:n.*615-74del
ENST00000692212.1:n.4591-74del
ENST00000692355.1:c.704-74del
ENST00000692413.1:c.1433-74del ENSP00000509374.1:n.1433-74del
ENST00000692825.1:c.1519-74del ENSP00000509447.1:n.1519-74del
ENST00000693308.1:c.1499-74del ENSP00000509770.1:n.1499-74del
ENST00000693763.1:n.2611-74del
ENST00000245407.8:c.1451-74del MANE Select ENSP00000245407.3:n.1451-74del
ENST00000245407.7:c.1451-74del ENSP00000245407.3:n.1451-74del
ENST00000435065.6:c.1523-74del ENSP00000402760.2:n.1523-74del
ENST00000447841.5:c.295-74del
ENST00000448810.5:c.713-74del
ENST00000461013.5:n.8873-74del
ENST00000475308.1:n.2129-74del
ENST00000479605.5:n.554-74del
NM_001308122.1:c.1523-74del NP_001295051.1:n.1523-74del
NM_003060.3:c.1451-74del NP_003051.1:n.1451-74del
XM_011543590.1:c.833-74del XP_011541892.1:n.833-74del
XR_948290.1:n.1577-74del
XM_011543590.2:c.833-74del XP_011541892.1:n.833-74del
XM_017009778.2:c.923-74del XP_016865267.1:n.923-74del
XR_001742215.1:n.1706-74del
XR_001742216.1:n.1725-74del
XR_427718.2:n.1811-74del
XR_948290.2:n.1577-74del
XR_948291.2:n.1805-74del
NM_003060.4:c.1451-74del MANE Select NP_003051.1:n.1451-74del
NM_001308122.2:c.1523-74del NP_001295051.1:n.1523-74del