Canonical Allele Identifier: CA2139919981

Gene: KIAA0586

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.58467821C= , CM000676.2:g.58467821C=	GRCh38
NC_000014.8:g.58934539C= , CM000676.1:g.58934539C=	GRCh37
NC_000014.7:g.58004292C=	NCBI36
NG_051335.2:g.45437C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619722.5:c.2086C=	ENSP00000481936.1:p.Pro696=
ENST00000650845.1:n.2887C=
ENST00000650904.1:c.2341C=	ENSP00000498606.1:p.Pro781=
ENST00000651759.1:c.1090C=	ENSP00000498415.1:p.Pro364=
ENST00000651937.1:c.*422C=	ENSP00000498785.1:n.*422C=
ENST00000652326.2:c.2341C= MANE Select	ENSP00000498929.1:p.Pro781=
ENST00000652414.1:c.445C=	ENSP00000498397.1:p.Pro149=
ENST00000652732.1:c.*1907C=	ENSP00000498799.1:n.*1907C=
ENST00000261244.9:c.2113C=	ENSP00000261244.5:p.Pro705=
ENST00000354386.10:c.2500C=	ENSP00000346359.6:p.Pro834=
ENST00000423743.7:c.2209C=	ENSP00000399427.3:p.Pro737=
ENST00000538571.6:n.1931C=
ENST00000556134.5:c.2209C=	ENSP00000452351.2:p.Pro737=
ENST00000619416.4:c.2296C=	ENSP00000478083.1:p.Pro766=
ENST00000619722.4:c.2086C=	ENSP00000481936.1:p.Pro696=
NM_001244189.1:c.2500C=	NP_001231118.1:p.Pro834=
NM_001244190.1:c.2296C=	NP_001231119.1:p.Pro766=
NM_001244191.1:c.2086C=	NP_001231120.1:p.Pro696=
NM_001244192.1:c.2209C=	NP_001231121.1:p.Pro737=
NM_001244193.1:c.1921C=	NP_001231122.1:p.Pro641=
NM_014749.3:c.2113C=	NP_055564.3:p.Pro705=
NM_001329943.2:c.2341C=	NP_001316872.1:p.Pro781=
NM_001329944.1:c.2341C=	NP_001316873.1:p.Pro781=
NM_001329945.1:c.2086C=	NP_001316874.1:p.Pro696=
NM_001329946.1:c.2341C=	NP_001316875.1:p.Pro781=
NM_001329947.1:c.2341C=	NP_001316876.1:p.Pro781=
NM_001364700.1:c.2086C=	NP_001351629.1:p.Pro696=
NM_001364701.1:c.2086C=	NP_001351630.1:p.Pro696=
NM_014749.4:c.2113C=	NP_055564.3:p.Pro705=
XM_024449779.1:c.2464C=	XP_024305547.1:p.Pro822=
XM_024449780.1:c.2365C=	XP_024305548.1:p.Pro789=
XM_024449781.1:c.2464C=	XP_024305549.1:p.Pro822=
XM_024449782.1:c.2110C=	XP_024305550.1:p.Pro704=
XM_024449783.1:c.2110C=	XP_024305551.1:p.Pro704=
XM_024449784.1:c.2110C=	XP_024305552.1:p.Pro704=
XM_024449785.1:c.2086C=	XP_024305553.1:p.Pro696=
XM_024449787.1:c.1945C=	XP_024305555.1:p.Pro649=
XM_024449788.1:c.1921C=	XP_024305556.1:p.Pro641=
XM_024449789.1:c.1921C=	XP_024305557.1:p.Pro641=
XM_024449791.1:c.2365C=	XP_024305559.1:p.Pro789=
NM_001244189.2:c.2500C=	NP_001231118.1:p.Pro834=
NM_001244190.2:c.2296C=	NP_001231119.1:p.Pro766=
NM_001244192.2:c.2209C=	NP_001231121.1:p.Pro737=
NM_001329943.3:c.2341C= MANE Select	NP_001316872.1:p.Pro781=
NM_001329944.2:c.2341C=	NP_001316873.1:p.Pro781=
NM_001329945.2:c.2086C=	NP_001316874.1:p.Pro696=
NM_001329946.2:c.2341C=	NP_001316875.1:p.Pro781=
NM_001329947.2:c.2341C=	NP_001316876.1:p.Pro781=
NM_001364701.2:c.2086C=	NP_001351630.1:p.Pro696=
NM_014749.5:c.2113C=	NP_055564.3:p.Pro705=
NM_001244191.2:c.2086C=	NP_001231120.1:p.Pro696=
NM_001244193.2:c.1921C=	NP_001231122.1:p.Pro641=