Canonical Allele Identifier: CA7051733

Gene: CARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.110642652C>T , CM000675.2:g.110642652C>T	GRCh38
NC_000013.10:g.111294999C>T , CM000675.1:g.111294999C>T	GRCh37
NC_000013.9:g.110093000C>T	NCBI36
NG_042045.1:g.68529G>A
NG_042045.2:g.75950G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_024537.4:c.1417-131G>A MANE Select	NP_078813.1:n.1417-131G>A
ENST00000257347.9:c.1417-131G>A MANE Select	ENSP00000257347.4:n.1417-131G>A
NM_001352252.1:c.631-131G>A	NP_001339181.1:n.631-131G>A
NM_001352252.2:c.631-131G>A	NP_001339181.1:n.631-131G>A
NM_024537.2:c.1417-131G>A	NP_078813.1:n.1417-131G>A
NM_024537.3:c.1417-131G>A	NP_078813.1:n.1417-131G>A
NR_147941.1:n.1501-131G>A
NR_147942.1:n.1900-131G>A
NR_147942.2:n.1836-131G>A
ENST00000257347.8:c.1417-131G>A	ENSP00000257347.4:n.1417-131G>A
ENST00000375781.9:n.2218G>A
ENST00000471986.2:n.108-155G>A
ENST00000480437.5:n.412-131G>A
ENST00000481787.6:n.851-131G>A
ENST00000487253.6:c.616-131G>A
ENST00000535516.5:n.1917-131G>A
ENST00000535615.5:n.701-131G>A
ENST00000537802.5:n.2829-131G>A
ENST00000540006.5:n.1082-131G>A
ENST00000541239.5:n.2982G>A
ENST00000542774.5:n.416-131G>A
XM_006719953.2:c.1078-131G>A	XP_006720016.1:n.1078-131G>A
XM_006719953.3:c.1078-131G>A	XP_006720016.1:n.1078-131G>A
XM_011521115.1:c.1078-131G>A	XP_011519417.1:n.1078-131G>A
XM_011521116.1:c.1072-131G>A	XP_011519418.1:n.1072-131G>A
XM_011521120.1:c.631-131G>A	XP_011519422.1:n.631-131G>A
XM_017020741.1:c.1078-131G>A	XP_016876230.1:n.1078-131G>A
XM_024449409.1:c.631-131G>A	XP_024305177.1:n.631-131G>A
XR_001749664.2:n.2116-131G>A
XR_001749665.2:n.1998-131G>A
XR_002957472.1:n.2523-131G>A
XR_243047.2:n.1558-131G>A
XR_243047.3:n.1575-131G>A
XR_243048.3:n.1563-131G>A
XR_243048.4:n.1580-131G>A
XR_243049.3:n.1681-131G>A
XR_243049.4:n.1698-131G>A
XR_243051.2:n.1373-131G>A
XR_243051.3:n.1390-131G>A