Canonical Allele Identifier: CA2139919849
Gene: KIAA0586 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.58467742C= , CM000676.2:g.58467742C= GRCh38
NC_000014.8:g.58934460C= , CM000676.1:g.58934460C= GRCh37
NC_000014.7:g.58004213C= NCBI36
NG_051335.2:g.45358C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000619722.5:c.2007C= ENSP00000481936.1:p.Thr669=
ENST00000650845.1:n.2808C=
ENST00000650904.1:c.2262C= ENSP00000498606.1:p.Thr754=
ENST00000651759.1:c.1011C= ENSP00000498415.1:p.Thr337=
ENST00000651937.1:c.*343C= ENSP00000498785.1:n.*343C=
ENST00000652326.2:c.2262C= MANE Select ENSP00000498929.1:p.Thr754=
ENST00000652414.1:c.366C= ENSP00000498397.1:p.Thr122=
ENST00000652732.1:c.*1828C= ENSP00000498799.1:n.*1828C=
ENST00000261244.9:c.2034C= ENSP00000261244.5:p.Thr678=
ENST00000354386.10:c.2421C= ENSP00000346359.6:p.Thr807=
ENST00000423743.7:c.2130C= ENSP00000399427.3:p.Thr710=
ENST00000538571.6:n.1852C=
ENST00000556134.5:c.2130C= ENSP00000452351.2:p.Thr710=
ENST00000619416.4:c.2217C= ENSP00000478083.1:p.Thr739=
ENST00000619722.4:c.2007C= ENSP00000481936.1:p.Thr669=
NM_001244189.1:c.2421C= NP_001231118.1:p.Thr807=
NM_001244190.1:c.2217C= NP_001231119.1:p.Thr739=
NM_001244191.1:c.2007C= NP_001231120.1:p.Thr669=
NM_001244192.1:c.2130C= NP_001231121.1:p.Thr710=
NM_001244193.1:c.1842C= NP_001231122.1:p.Thr614=
NM_014749.3:c.2034C= NP_055564.3:p.Thr678=
NM_001329943.2:c.2262C= NP_001316872.1:p.Thr754=
NM_001329944.1:c.2262C= NP_001316873.1:p.Thr754=
NM_001329945.1:c.2007C= NP_001316874.1:p.Thr669=
NM_001329946.1:c.2262C= NP_001316875.1:p.Thr754=
NM_001329947.1:c.2262C= NP_001316876.1:p.Thr754=
NM_001364700.1:c.2007C= NP_001351629.1:p.Thr669=
NM_001364701.1:c.2007C= NP_001351630.1:p.Thr669=
NM_014749.4:c.2034C= NP_055564.3:p.Thr678=
XM_024449779.1:c.2385C= XP_024305547.1:p.Thr795=
XM_024449780.1:c.2286C= XP_024305548.1:p.Thr762=
XM_024449781.1:c.2385C= XP_024305549.1:p.Thr795=
XM_024449782.1:c.2031C= XP_024305550.1:p.Thr677=
XM_024449783.1:c.2031C= XP_024305551.1:p.Thr677=
XM_024449784.1:c.2031C= XP_024305552.1:p.Thr677=
XM_024449785.1:c.2007C= XP_024305553.1:p.Thr669=
XM_024449787.1:c.1866C= XP_024305555.1:p.Thr622=
XM_024449788.1:c.1842C= XP_024305556.1:p.Thr614=
XM_024449789.1:c.1842C= XP_024305557.1:p.Thr614=
XM_024449791.1:c.2286C= XP_024305559.1:p.Thr762=
NM_001244189.2:c.2421C= NP_001231118.1:p.Thr807=
NM_001244190.2:c.2217C= NP_001231119.1:p.Thr739=
NM_001244192.2:c.2130C= NP_001231121.1:p.Thr710=
NM_001329943.3:c.2262C= MANE Select NP_001316872.1:p.Thr754=
NM_001329944.2:c.2262C= NP_001316873.1:p.Thr754=
NM_001329945.2:c.2007C= NP_001316874.1:p.Thr669=
NM_001329946.2:c.2262C= NP_001316875.1:p.Thr754=
NM_001329947.2:c.2262C= NP_001316876.1:p.Thr754=
NM_001364701.2:c.2007C= NP_001351630.1:p.Thr669=
NM_014749.5:c.2034C= NP_055564.3:p.Thr678=
NM_001244191.2:c.2007C= NP_001231120.1:p.Thr669=
NM_001244193.2:c.1842C= NP_001231122.1:p.Thr614=