Canonical Allele Identifier: CA2625061298
Gene: KIAA0586 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.58467726del , CM000676.2:g.58467726del GRCh38
NC_000014.8:g.58934444del , CM000676.1:g.58934444del GRCh37
NC_000014.7:g.58004197del NCBI36
NG_051335.2:g.45342del

Transcript Alleles

HGVS Amino-acid Change
ENST00000619722.5:c.2000-9del ENSP00000481936.1:n.2000-9del
ENST00000650845.1:n.2801-9del
ENST00000650904.1:c.2255-9del ENSP00000498606.1:n.2255-9del
ENST00000651759.1:c.1004-9del ENSP00000498415.1:n.1004-9del
ENST00000651937.1:c.*336-9del ENSP00000498785.1:n.*336-9del
ENST00000652326.2:c.2255-9del MANE Select ENSP00000498929.1:n.2255-9del
ENST00000652414.1:c.359-9del ENSP00000498397.1:n.359-9del
ENST00000652732.1:c.*1821-9del ENSP00000498799.1:n.*1821-9del
ENST00000261244.9:c.2027-9del ENSP00000261244.5:n.2027-9del
ENST00000354386.10:c.2414-9del ENSP00000346359.6:n.2414-9del
ENST00000423743.7:c.2123-9del ENSP00000399427.3:n.2123-9del
ENST00000538571.6:n.1845-9del
ENST00000556134.5:c.2123-9del ENSP00000452351.2:n.2123-9del
ENST00000619416.4:c.2210-9del ENSP00000478083.1:n.2210-9del
ENST00000619722.4:c.2000-9del ENSP00000481936.1:n.2000-9del
NM_001244189.1:c.2414-9del NP_001231118.1:n.2414-9del
NM_001244190.1:c.2210-9del NP_001231119.1:n.2210-9del
NM_001244191.1:c.2000-9del NP_001231120.1:n.2000-9del
NM_001244192.1:c.2123-9del NP_001231121.1:n.2123-9del
NM_001244193.1:c.1835-9del NP_001231122.1:n.1835-9del
NM_014749.3:c.2027-9del NP_055564.3:n.2027-9del
NM_001329943.2:c.2255-9del NP_001316872.1:n.2255-9del
NM_001329944.1:c.2255-9del NP_001316873.1:n.2255-9del
NM_001329945.1:c.2000-9del NP_001316874.1:n.2000-9del
NM_001329946.1:c.2255-9del NP_001316875.1:n.2255-9del
NM_001329947.1:c.2255-9del NP_001316876.1:n.2255-9del
NM_001364700.1:c.2000-9del NP_001351629.1:n.2000-9del
NM_001364701.1:c.2000-9del NP_001351630.1:n.2000-9del
NM_014749.4:c.2027-9del NP_055564.3:n.2027-9del
XM_024449779.1:c.2378-9del XP_024305547.1:n.2378-9del
XM_024449780.1:c.2279-9del XP_024305548.1:n.2279-9del
XM_024449781.1:c.2378-9del XP_024305549.1:n.2378-9del
XM_024449782.1:c.2024-9del XP_024305550.1:n.2024-9del
XM_024449783.1:c.2024-9del XP_024305551.1:n.2024-9del
XM_024449784.1:c.2024-9del XP_024305552.1:n.2024-9del
XM_024449785.1:c.2000-9del XP_024305553.1:n.2000-9del
XM_024449787.1:c.1859-9del XP_024305555.1:n.1859-9del
XM_024449788.1:c.1835-9del XP_024305556.1:n.1835-9del
XM_024449789.1:c.1835-9del XP_024305557.1:n.1835-9del
XM_024449791.1:c.2279-9del XP_024305559.1:n.2279-9del
NM_001244189.2:c.2414-9del NP_001231118.1:n.2414-9del
NM_001244190.2:c.2210-9del NP_001231119.1:n.2210-9del
NM_001244192.2:c.2123-9del NP_001231121.1:n.2123-9del
NM_001329943.3:c.2255-9del MANE Select NP_001316872.1:n.2255-9del
NM_001329944.2:c.2255-9del NP_001316873.1:n.2255-9del
NM_001329945.2:c.2000-9del NP_001316874.1:n.2000-9del
NM_001329946.2:c.2255-9del NP_001316875.1:n.2255-9del
NM_001329947.2:c.2255-9del NP_001316876.1:n.2255-9del
NM_001364701.2:c.2000-9del NP_001351630.1:n.2000-9del
NM_014749.5:c.2027-9del NP_055564.3:n.2027-9del
NM_001244191.2:c.2000-9del NP_001231120.1:n.2000-9del
NM_001244193.2:c.1835-9del NP_001231122.1:n.1835-9del