Canonical Allele Identifier: CA389875137

Gene: KIAA0586

Linked Data

• MyVariant Identifiers: chr14:g.58934512C>G (hg19) ; chr14:g.58467794C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.58467794C>G , CM000676.2:g.58467794C>G	GRCh38
NC_000014.8:g.58934512C>G , CM000676.1:g.58934512C>G	GRCh37
NC_000014.7:g.58004265C>G	NCBI36
NG_051335.2:g.45410C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000619722.5:c.2059C>G	ENSP00000481936.1:p.His687Asp
ENST00000650845.1:n.2860C>G
ENST00000650904.1:c.2314C>G	ENSP00000498606.1:p.His772Asp
ENST00000651759.1:c.1063C>G	ENSP00000498415.1:p.His355Asp
ENST00000651937.1:c.*395C>G	ENSP00000498785.1:n.*395C>G
ENST00000652326.2:c.2314C>G MANE Select	ENSP00000498929.1:p.His772Asp
ENST00000652414.1:c.418C>G	ENSP00000498397.1:p.His140Asp
ENST00000652732.1:c.*1880C>G	ENSP00000498799.1:n.*1880C>G
ENST00000261244.9:c.2086C>G	ENSP00000261244.5:p.His696Asp
ENST00000354386.10:c.2473C>G	ENSP00000346359.6:p.His825Asp
ENST00000423743.7:c.2182C>G	ENSP00000399427.3:p.His728Asp
ENST00000538571.6:n.1904C>G
ENST00000556134.5:c.2182C>G	ENSP00000452351.2:p.His728Asp
ENST00000619416.4:c.2269C>G	ENSP00000478083.1:p.His757Asp
ENST00000619722.4:c.2059C>G	ENSP00000481936.1:p.His687Asp
NM_001244189.1:c.2473C>G	NP_001231118.1:p.His825Asp
NM_001244190.1:c.2269C>G	NP_001231119.1:p.His757Asp
NM_001244191.1:c.2059C>G	NP_001231120.1:p.His687Asp
NM_001244192.1:c.2182C>G	NP_001231121.1:p.His728Asp
NM_001244193.1:c.1894C>G	NP_001231122.1:p.His632Asp
NM_014749.3:c.2086C>G	NP_055564.3:p.His696Asp
NM_001329943.2:c.2314C>G	NP_001316872.1:p.His772Asp
NM_001329944.1:c.2314C>G	NP_001316873.1:p.His772Asp
NM_001329945.1:c.2059C>G	NP_001316874.1:p.His687Asp
NM_001329946.1:c.2314C>G	NP_001316875.1:p.His772Asp
NM_001329947.1:c.2314C>G	NP_001316876.1:p.His772Asp
NM_001364700.1:c.2059C>G	NP_001351629.1:p.His687Asp
NM_001364701.1:c.2059C>G	NP_001351630.1:p.His687Asp
NM_014749.4:c.2086C>G	NP_055564.3:p.His696Asp
XM_024449779.1:c.2437C>G	XP_024305547.1:p.His813Asp
XM_024449780.1:c.2338C>G	XP_024305548.1:p.His780Asp
XM_024449781.1:c.2437C>G	XP_024305549.1:p.His813Asp
XM_024449782.1:c.2083C>G	XP_024305550.1:p.His695Asp
XM_024449783.1:c.2083C>G	XP_024305551.1:p.His695Asp
XM_024449784.1:c.2083C>G	XP_024305552.1:p.His695Asp
XM_024449785.1:c.2059C>G	XP_024305553.1:p.His687Asp
XM_024449787.1:c.1918C>G	XP_024305555.1:p.His640Asp
XM_024449788.1:c.1894C>G	XP_024305556.1:p.His632Asp
XM_024449789.1:c.1894C>G	XP_024305557.1:p.His632Asp
XM_024449791.1:c.2338C>G	XP_024305559.1:p.His780Asp
NM_001244189.2:c.2473C>G	NP_001231118.1:p.His825Asp
NM_001244190.2:c.2269C>G	NP_001231119.1:p.His757Asp
NM_001244192.2:c.2182C>G	NP_001231121.1:p.His728Asp
NM_001329943.3:c.2314C>G MANE Select	NP_001316872.1:p.His772Asp
NM_001329944.2:c.2314C>G	NP_001316873.1:p.His772Asp
NM_001329945.2:c.2059C>G	NP_001316874.1:p.His687Asp
NM_001329946.2:c.2314C>G	NP_001316875.1:p.His772Asp
NM_001329947.2:c.2314C>G	NP_001316876.1:p.His772Asp
NM_001364701.2:c.2059C>G	NP_001351630.1:p.His687Asp
NM_014749.5:c.2086C>G	NP_055564.3:p.His696Asp
NM_001244191.2:c.2059C>G	NP_001231120.1:p.His687Asp
NM_001244193.2:c.1894C>G	NP_001231122.1:p.His632Asp