Canonical Allele Identifier: CA388744468

Gene: CARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110647516_110647517insGGA , CM000675.2:g.110647516_110647517insGGA	GRCh38
NC_000013.10:g.111299863_111299864insGGA , CM000675.1:g.111299863_111299864insGGA	GRCh37
NC_000013.9:g.110097864_110097865insGGA	NCBI36
NG_042045.1:g.63664_63665insTCC
NG_042045.2:g.71085_71086insTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257347.9:c.1055-278_1055-277insTCC MANE Select	ENSP00000257347.4:n.1055-278_1055-277insTCC
ENST00000257347.8:c.1055-278_1055-277insTCC	ENSP00000257347.4:n.1055-278_1055-277insTCC
ENST00000375781.9:n.326-278_326-277insTCC
ENST00000481787.6:n.489-278_489-277insTCC
ENST00000487253.6:c.136-278_136-277insTCC
ENST00000535398.5:n.1247-278_1247-277insTCC
ENST00000535516.5:n.545-278_545-277insTCC
ENST00000535615.5:n.339-278_339-277insTCC
ENST00000537386.1:n.179-278_179-277insTCC
ENST00000537404.1:n.175-278_175-277insTCC
ENST00000537802.5:n.1339-278_1339-277insTCC
ENST00000540006.5:n.479-278_479-277insTCC
ENST00000541362.5:n.279-278_279-277insTCC
ENST00000543487.5:n.571-278_571-277insTCC
ENST00000545506.5:n.400-278_400-277insTCC
NM_024537.2:c.1055-278_1055-277insTCC	NP_078813.1:n.1055-278_1055-277insTCC
NM_024537.3:c.1055-278_1055-277insTCC	NP_078813.1:n.1055-278_1055-277insTCC
XM_006719953.2:c.716-278_716-277insTCC	XP_006720016.1:n.716-278_716-277insTCC
XM_011521114.1:c.1055-278_1055-277insTCC	XP_011519416.1:n.1055-278_1055-277insTCC
XM_011521115.1:c.716-278_716-277insTCC	XP_011519417.1:n.716-278_716-277insTCC
XM_011521116.1:c.710-278_710-277insTCC	XP_011519418.1:n.710-278_710-277insTCC
XM_011521120.1:c.269-278_269-277insTCC	XP_011519422.1:n.269-278_269-277insTCC
XR_243047.2:n.1078-278_1078-277insTCC
XR_243048.3:n.1078-278_1078-277insTCC
XR_243049.3:n.1078-278_1078-277insTCC
XR_243051.2:n.1011-278_1011-277insTCC
NM_001352252.1:c.269-278_269-277insTCC	NP_001339181.1:n.269-278_269-277insTCC
NR_147941.1:n.1026-278_1026-277insTCC
NR_147942.1:n.1300-278_1300-277insTCC
XM_006719953.3:c.716-278_716-277insTCC	XP_006720016.1:n.716-278_716-277insTCC
XM_017020741.1:c.716-278_716-277insTCC	XP_016876230.1:n.716-278_716-277insTCC
XM_017020742.2:c.988-278_988-277insTCC	XP_016876231.1:n.988-278_988-277insTCC
XM_024449409.1:c.269-278_269-277insTCC	XP_024305177.1:n.269-278_269-277insTCC
XR_001749664.2:n.1095-278_1095-277insTCC
XR_001749665.2:n.1095-278_1095-277insTCC
XR_001749666.2:n.1095-278_1095-277insTCC
XR_001749667.2:n.1095-278_1095-277insTCC
XR_001749668.2:n.1028-278_1028-277insTCC
XR_002957472.1:n.1028-278_1028-277insTCC
XR_243047.3:n.1095-278_1095-277insTCC
XR_243048.4:n.1095-278_1095-277insTCC
XR_243049.4:n.1095-278_1095-277insTCC
XR_243051.3:n.1028-278_1028-277insTCC
NM_024537.4:c.1055-278_1055-277insTCC MANE Select	NP_078813.1:n.1055-278_1055-277insTCC
NR_147942.2:n.1236-278_1236-277insTCC
NM_001352252.2:c.269-278_269-277insTCC	NP_001339181.1:n.269-278_269-277insTCC