Canonical Allele Identifier: CA2839171675

Gene: KIAA0586

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.58444079_58444080insCA , CM000676.2:g.58444079_58444080insCA	GRCh38
NC_000014.8:g.58910797_58910798insCA , CM000676.1:g.58910797_58910798insCA	GRCh37
NC_000014.7:g.57980550_57980551insCA	NCBI36
NG_051335.2:g.21695_21696insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555203.6:n.401_402insCA
ENST00000619722.5:c.456_457insCA	ENSP00000481936.1:p.Leu153HisfsTer11
ENST00000650845.1:n.1257_1258insCA
ENST00000650904.1:c.711_712insCA	ENSP00000498606.1:p.Leu238HisfsTer11
ENST00000651937.1:c.666_667insCA	ENSP00000498785.1:p.Leu223HisfsTer11
ENST00000652120.1:n.617_618insCA
ENST00000652326.2:c.711_712insCA MANE Select	ENSP00000498929.1:p.Leu238HisfsTer11
ENST00000652732.1:c.*277_*278insCA	ENSP00000498799.1:n.*277_*278insCA
ENST00000674802.1:n.943_944insCA
ENST00000261244.9:c.711_712insCA	ENSP00000261244.5:p.Leu238HisfsTer11
ENST00000354386.10:c.870_871insCA	ENSP00000346359.6:p.Leu291HisfsTer11
ENST00000423743.7:c.579_580insCA	ENSP00000399427.3:p.Leu194HisfsTer11
ENST00000538571.6:n.301_302insCA
ENST00000555833.5:c.456_457insCA	ENSP00000450855.1:p.Leu153HisfsTer11
ENST00000556134.5:c.579_580insCA	ENSP00000452351.2:p.Leu194HisfsTer11
ENST00000619416.4:c.666_667insCA	ENSP00000478083.1:p.Leu223HisfsTer11
ENST00000619722.4:c.456_457insCA	ENSP00000481936.1:p.Leu153HisfsTer11
NM_001244189.1:c.870_871insCA	NP_001231118.1:p.Leu291HisfsTer11
NM_001244190.1:c.666_667insCA	NP_001231119.1:p.Leu223HisfsTer11
NM_001244191.1:c.456_457insCA	NP_001231120.1:p.Leu153HisfsTer11
NM_001244192.1:c.579_580insCA	NP_001231121.1:p.Leu194HisfsTer11
NM_001244193.1:c.291_292insCA	NP_001231122.1:p.Leu98HisfsTer11
NM_014749.3:c.711_712insCA	NP_055564.3:p.Leu238HisfsTer11
NM_001329943.2:c.711_712insCA	NP_001316872.1:p.Leu238HisfsTer11
NM_001329944.1:c.711_712insCA	NP_001316873.1:p.Leu238HisfsTer11
NM_001329945.1:c.456_457insCA	NP_001316874.1:p.Leu153HisfsTer11
NM_001329946.1:c.711_712insCA	NP_001316875.1:p.Leu238HisfsTer11
NM_001329947.1:c.711_712insCA	NP_001316876.1:p.Leu238HisfsTer11
NM_001364700.1:c.456_457insCA	NP_001351629.1:p.Leu153HisfsTer11
NM_001364701.1:c.456_457insCA	NP_001351630.1:p.Leu153HisfsTer11
NM_014749.4:c.711_712insCA	NP_055564.3:p.Leu238HisfsTer11
XM_024449779.1:c.834_835insCA	XP_024305547.1:p.Leu279HisfsTer11
XM_024449780.1:c.711_712insCA	XP_024305548.1:p.Leu238HisfsTer11
XM_024449781.1:c.834_835insCA	XP_024305549.1:p.Leu279HisfsTer11
XM_024449782.1:c.456_457insCA	XP_024305550.1:p.Leu153HisfsTer11
XM_024449783.1:c.456_457insCA	XP_024305551.1:p.Leu153HisfsTer11
XM_024449784.1:c.456_457insCA	XP_024305552.1:p.Leu153HisfsTer11
XM_024449785.1:c.456_457insCA	XP_024305553.1:p.Leu153HisfsTer11
XM_024449787.1:c.315_316insCA	XP_024305555.1:p.Leu106HisfsTer11
XM_024449788.1:c.291_292insCA	XP_024305556.1:p.Leu98HisfsTer11
XM_024449789.1:c.291_292insCA	XP_024305557.1:p.Leu98HisfsTer11
XM_024449791.1:c.711_712insCA	XP_024305559.1:p.Leu238HisfsTer11
NM_001244189.2:c.870_871insCA	NP_001231118.1:p.Leu291HisfsTer11
NM_001244190.2:c.666_667insCA	NP_001231119.1:p.Leu223HisfsTer11
NM_001244192.2:c.579_580insCA	NP_001231121.1:p.Leu194HisfsTer11
NM_001329943.3:c.711_712insCA MANE Select	NP_001316872.1:p.Leu238HisfsTer11
NM_001329944.2:c.711_712insCA	NP_001316873.1:p.Leu238HisfsTer11
NM_001329945.2:c.456_457insCA	NP_001316874.1:p.Leu153HisfsTer11
NM_001329946.2:c.711_712insCA	NP_001316875.1:p.Leu238HisfsTer11
NM_001329947.2:c.711_712insCA	NP_001316876.1:p.Leu238HisfsTer11
NM_001364701.2:c.456_457insCA	NP_001351630.1:p.Leu153HisfsTer11
NM_014749.5:c.711_712insCA	NP_055564.3:p.Leu238HisfsTer11
NM_001244191.2:c.456_457insCA	NP_001231120.1:p.Leu153HisfsTer11
NM_001244193.2:c.291_292insCA	NP_001231122.1:p.Leu98HisfsTer11