Canonical Allele Identifier: CA2139904876
Gene: KIAA0586 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.58444126A= , CM000676.2:g.58444126A= GRCh38
NC_000014.8:g.58910844A= , CM000676.1:g.58910844A= GRCh37
NC_000014.7:g.57980597A= NCBI36
NG_051335.2:g.21742A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555203.6:n.448A=
ENST00000619722.5:c.503A= ENSP00000481936.1:p.Gln168=
ENST00000650845.1:n.1304A=
ENST00000650904.1:c.758A= ENSP00000498606.1:p.Gln253=
ENST00000651937.1:c.713A= ENSP00000498785.1:p.Gln238=
ENST00000652120.1:n.664A=
ENST00000652326.2:c.758A= MANE Select ENSP00000498929.1:p.Gln253=
ENST00000652732.1:c.*324A= ENSP00000498799.1:n.*324A=
ENST00000674802.1:n.990A=
ENST00000261244.9:c.758A= ENSP00000261244.5:p.Gln253=
ENST00000354386.10:c.917A= ENSP00000346359.6:p.Gln306=
ENST00000423743.7:c.626A= ENSP00000399427.3:p.Gln209=
ENST00000538571.6:n.348A=
ENST00000555833.5:c.503A= ENSP00000450855.1:p.Gln168=
ENST00000556134.5:c.626A= ENSP00000452351.2:p.Gln209=
ENST00000619416.4:c.713A= ENSP00000478083.1:p.Gln238=
ENST00000619722.4:c.503A= ENSP00000481936.1:p.Gln168=
NM_001244189.1:c.917A= NP_001231118.1:p.Gln306=
NM_001244190.1:c.713A= NP_001231119.1:p.Gln238=
NM_001244191.1:c.503A= NP_001231120.1:p.Gln168=
NM_001244192.1:c.626A= NP_001231121.1:p.Gln209=
NM_001244193.1:c.338A= NP_001231122.1:p.Gln113=
NM_014749.3:c.758A= NP_055564.3:p.Gln253=
NM_001329943.2:c.758A= NP_001316872.1:p.Gln253=
NM_001329944.1:c.758A= NP_001316873.1:p.Gln253=
NM_001329945.1:c.503A= NP_001316874.1:p.Gln168=
NM_001329946.1:c.758A= NP_001316875.1:p.Gln253=
NM_001329947.1:c.758A= NP_001316876.1:p.Gln253=
NM_001364700.1:c.503A= NP_001351629.1:p.Gln168=
NM_001364701.1:c.503A= NP_001351630.1:p.Gln168=
NM_014749.4:c.758A= NP_055564.3:p.Gln253=
XM_024449779.1:c.881A= XP_024305547.1:p.Gln294=
XM_024449780.1:c.758A= XP_024305548.1:p.Gln253=
XM_024449781.1:c.881A= XP_024305549.1:p.Gln294=
XM_024449782.1:c.503A= XP_024305550.1:p.Gln168=
XM_024449783.1:c.503A= XP_024305551.1:p.Gln168=
XM_024449784.1:c.503A= XP_024305552.1:p.Gln168=
XM_024449785.1:c.503A= XP_024305553.1:p.Gln168=
XM_024449787.1:c.362A= XP_024305555.1:p.Gln121=
XM_024449788.1:c.338A= XP_024305556.1:p.Gln113=
XM_024449789.1:c.338A= XP_024305557.1:p.Gln113=
XM_024449791.1:c.758A= XP_024305559.1:p.Gln253=
NM_001244189.2:c.917A= NP_001231118.1:p.Gln306=
NM_001244190.2:c.713A= NP_001231119.1:p.Gln238=
NM_001244192.2:c.626A= NP_001231121.1:p.Gln209=
NM_001329943.3:c.758A= MANE Select NP_001316872.1:p.Gln253=
NM_001329944.2:c.758A= NP_001316873.1:p.Gln253=
NM_001329945.2:c.503A= NP_001316874.1:p.Gln168=
NM_001329946.2:c.758A= NP_001316875.1:p.Gln253=
NM_001329947.2:c.758A= NP_001316876.1:p.Gln253=
NM_001364701.2:c.503A= NP_001351630.1:p.Gln168=
NM_014749.5:c.758A= NP_055564.3:p.Gln253=
NM_001244191.2:c.503A= NP_001231120.1:p.Gln168=
NM_001244193.2:c.338A= NP_001231122.1:p.Gln113=