Canonical Allele Identifier: CA2677183431

Gene: FARS2

Linked Data

• gnomAD v4: 6-5613154-CTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.5613156_5613158del , CM000668.2:g.5613156_5613158del	GRCh38
NC_000006.11:g.5613389_5613391del , CM000668.1:g.5613389_5613391del	GRCh37
NC_000006.10:g.5558388_5558390del	NCBI36
NG_033003.1:g.356806_356808del
NG_033003.2:g.356806_356808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274680.9:c.1066-13_1066-11del MANE Select	ENSP00000274680.4:n.1066-13_1066-11del
ENST00000648580.1:c.1066-13_1066-11del	ENSP00000497889.1:n.1066-13_1066-11del
ENST00000274680.8:c.1066-13_1066-11del	ENSP00000274680.3:n.1066-13_1066-11del
ENST00000324331.10:c.1066-13_1066-11del	ENSP00000316335.5:n.1066-13_1066-11del
NM_006567.3:c.1066-13_1066-11del	NP_006558.1:n.1066-13_1066-11del
XM_005248811.1:c.1066-13_1066-11del	XP_005248868.1:n.1066-13_1066-11del
XM_005248812.2:c.1066-13_1066-11del	XP_005248869.1:n.1066-13_1066-11del
XM_011514247.1:c.1066-13_1066-11del	XP_011512549.1:n.1066-13_1066-11del
XM_011514248.1:c.1066-13_1066-11del	XP_011512550.1:n.1066-13_1066-11del
XM_011514249.1:c.1066-13_1066-11del	XP_011512551.1:n.1066-13_1066-11del
XR_926026.1:n.2040-13_2040-11del
XR_926028.1:n.1529-13_1529-11del
NM_001318872.1:c.1066-13_1066-11del	NP_001305801.1:n.1066-13_1066-11del
NM_006567.4:c.1066-13_1066-11del	NP_006558.1:n.1066-13_1066-11del
XM_005248812.3:c.1066-13_1066-11del	XP_005248869.1:n.1066-13_1066-11del
XM_011514247.3:c.1066-13_1066-11del	XP_011512549.1:n.1066-13_1066-11del
XM_011514248.3:c.1066-13_1066-11del	XP_011512550.1:n.1066-13_1066-11del
XM_011514249.2:c.1066-13_1066-11del	XP_011512551.1:n.1066-13_1066-11del
XM_017010186.1:c.1066-13_1066-11del	XP_016865675.1:n.1066-13_1066-11del
XM_017010187.1:c.1066-13_1066-11del	XP_016865676.1:n.1066-13_1066-11del
XR_926028.2:n.1506-13_1506-11del
NM_001318872.2:c.1066-13_1066-11del	NP_001305801.1:n.1066-13_1066-11del
NM_001374875.1:c.1066-13_1066-11del	NP_001361804.1:n.1066-13_1066-11del
NM_001374876.1:c.1066-13_1066-11del	NP_001361805.1:n.1066-13_1066-11del
NM_001374877.1:c.1066-13_1066-11del	NP_001361806.1:n.1066-13_1066-11del
NM_001374878.1:c.1066-13_1066-11del	NP_001361807.1:n.1066-13_1066-11del
NM_001374879.1:c.1066-13_1066-11del	NP_001361808.1:n.1066-13_1066-11del
NM_001375257.1:c.1066-13_1066-11del	NP_001362186.1:n.1066-13_1066-11del
NM_001375258.1:c.934-13_934-11del	NP_001362187.1:n.934-13_934-11del
NM_001375259.1:c.370-13_370-11del	NP_001362188.1:n.370-13_370-11del
NM_001375260.1:c.370-13_370-11del	NP_001362189.1:n.370-13_370-11del
NM_006567.5:c.1066-13_1066-11del MANE Select	NP_006558.1:n.1066-13_1066-11del