Canonical Allele Identifier: CA612640552

Gene: CARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110644493A>T , CM000675.2:g.110644493A>T	GRCh38
NC_000013.10:g.111296840A>T , CM000675.1:g.111296840A>T	GRCh37
NC_000013.9:g.110094841A>T	NCBI36
NG_042045.1:g.66688T>A
NG_042045.2:g.74109T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257347.9:c.1318-10T>A MANE Select	ENSP00000257347.4:n.1318-10T>A
ENST00000257347.8:c.1318-10T>A	ENSP00000257347.4:n.1318-10T>A
ENST00000375781.9:n.589-10T>A
ENST00000471986.2:n.107+1474T>A
ENST00000480437.5:n.313-10T>A
ENST00000481787.6:n.752-10T>A
ENST00000487253.6:c.399-10T>A
ENST00000535398.5:n.1637-10T>A
ENST00000535516.5:n.1818-10T>A
ENST00000535615.5:n.602-10T>A
ENST00000537802.5:n.2612-10T>A
ENST00000540006.5:n.855T>A
ENST00000540215.1:n.524T>A
ENST00000541239.5:n.1141T>A
ENST00000542774.5:n.189T>A
ENST00000620794.1:c.140-10T>A
NM_024537.2:c.1318-10T>A	NP_078813.1:n.1318-10T>A
NM_024537.3:c.1318-10T>A	NP_078813.1:n.1318-10T>A
XM_006719953.2:c.979-10T>A	XP_006720016.1:n.979-10T>A
XM_011521115.1:c.979-10T>A	XP_011519417.1:n.979-10T>A
XM_011521116.1:c.973-10T>A	XP_011519418.1:n.973-10T>A
XM_011521120.1:c.532-10T>A	XP_011519422.1:n.532-10T>A
XR_243047.2:n.1341-10T>A
XR_243048.3:n.1454T>A
XR_243049.3:n.1454T>A
XR_243051.2:n.1274-10T>A
NM_001352252.1:c.532-10T>A	NP_001339181.1:n.532-10T>A
NR_147941.1:n.1289-10T>A
NR_147942.1:n.1673T>A
XM_006719953.3:c.979-10T>A	XP_006720016.1:n.979-10T>A
XM_017020741.1:c.979-10T>A	XP_016876230.1:n.979-10T>A
XM_024449409.1:c.532-10T>A	XP_024305177.1:n.532-10T>A
XR_001749664.2:n.1899-10T>A
XR_001749665.2:n.1899-10T>A
XR_001749666.2:n.2012T>A
XR_001749667.2:n.1358-10T>A
XR_001749668.2:n.1291-10T>A
XR_002957472.1:n.2414T>A
XR_243047.3:n.1358-10T>A
XR_243048.4:n.1471T>A
XR_243049.4:n.1471T>A
XR_243051.3:n.1291-10T>A
NM_024537.4:c.1318-10T>A MANE Select	NP_078813.1:n.1318-10T>A
NR_147942.2:n.1609T>A
NM_001352252.2:c.532-10T>A	NP_001339181.1:n.532-10T>A