Canonical Allele Identifier: CA1607612182

Gene: FARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.5404787_5404802delinsTCATATTTTGAAATTC , CM000668.2:g.5404787_5404802delinsTCATATTTTGAAATTC	GRCh38
NC_000006.11:g.5405020_5405035delinsTCATATTTTGAAATTC , CM000668.1:g.5405020_5405035delinsTCATATTTTGAAATTC	GRCh37
NC_000006.10:g.5350019_5350034delinsTCATATTTTGAAATTC	NCBI36
NG_033003.1:g.148437_148452delinsTCATATTTTGAAATTC
NG_033003.2:g.148437_148452delinsTCATATTTTGAAATTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274680.9:c.772+86_772+101delinsTCATATTTTGAAATTC MANE Select	ENSP00000274680.4:n.772+86_772+101delinsTCATATTTTGAAATTC
ENST00000648580.1:c.772+86_772+101delinsTCATATTTTGAAATTC	ENSP00000497889.1:n.772+86_772+101delinsTCATATTTTGAAATTC
ENST00000274680.8:c.772+86_772+101delinsTCATATTTTGAAATTC	ENSP00000274680.3:n.772+86_772+101delinsTCATATTTTGAAATTC
ENST00000324331.10:c.772+86_772+101delinsTCATATTTTGAAATTC	ENSP00000316335.5:n.772+86_772+101delinsTCATATTTTGAAATTC
ENST00000445533.1:c.160+86_160+101delinsTCATATTTTGAAATTC	ENSP00000392525.1:n.160+86_160+101delinsTCATATTTTGAAATTC
NM_006567.3:c.772+86_772+101delinsTCATATTTTGAAATTC	NP_006558.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_005248811.1:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_005248868.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_005248812.2:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_005248869.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_006714966.1:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_006715029.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_011514247.1:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_011512549.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_011514248.1:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_011512550.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_011514249.1:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_011512551.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_011514250.1:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_011512552.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_011514251.1:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_011512553.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XR_926026.1:n.1103+86_1103+101delinsTCATATTTTGAAATTC
XR_926027.1:n.1103+86_1103+101delinsTCATATTTTGAAATTC
XR_926028.1:n.1103+86_1103+101delinsTCATATTTTGAAATTC
NM_001318872.1:c.772+86_772+101delinsTCATATTTTGAAATTC	NP_001305801.1:n.772+86_772+101delinsTCATATTTTGAAATTC
NM_006567.4:c.772+86_772+101delinsTCATATTTTGAAATTC	NP_006558.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_005248812.3:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_005248869.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_006714966.3:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_006715029.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_011514247.3:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_011512549.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_011514248.3:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_011512550.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_011514249.2:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_011512551.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_011514251.3:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_011512553.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_017010186.1:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_016865675.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XM_017010187.1:c.772+86_772+101delinsTCATATTTTGAAATTC	XP_016865676.1:n.772+86_772+101delinsTCATATTTTGAAATTC
XR_926027.3:n.1080+86_1080+101delinsTCATATTTTGAAATTC
XR_926028.2:n.1080+86_1080+101delinsTCATATTTTGAAATTC
NM_001318872.2:c.772+86_772+101delinsTCATATTTTGAAATTC	NP_001305801.1:n.772+86_772+101delinsTCATATTTTGAAATTC
NM_001374875.1:c.772+86_772+101delinsTCATATTTTGAAATTC	NP_001361804.1:n.772+86_772+101delinsTCATATTTTGAAATTC
NM_001374876.1:c.772+86_772+101delinsTCATATTTTGAAATTC	NP_001361805.1:n.772+86_772+101delinsTCATATTTTGAAATTC
NM_001374877.1:c.772+86_772+101delinsTCATATTTTGAAATTC	NP_001361806.1:n.772+86_772+101delinsTCATATTTTGAAATTC
NM_001374878.1:c.772+86_772+101delinsTCATATTTTGAAATTC	NP_001361807.1:n.772+86_772+101delinsTCATATTTTGAAATTC
NM_001374879.1:c.772+86_772+101delinsTCATATTTTGAAATTC	NP_001361808.1:n.772+86_772+101delinsTCATATTTTGAAATTC
NM_001375257.1:c.772+86_772+101delinsTCATATTTTGAAATTC	NP_001362186.1:n.772+86_772+101delinsTCATATTTTGAAATTC
NM_001375258.1:c.772+86_772+101delinsTCATATTTTGAAATTC	NP_001362187.1:n.772+86_772+101delinsTCATATTTTGAAATTC
NM_001375259.1:c.76+86_76+101delinsTCATATTTTGAAATTC	NP_001362188.1:n.76+86_76+101delinsTCATATTTTGAAATTC
NM_001375260.1:c.76+86_76+101delinsTCATATTTTGAAATTC	NP_001362189.1:n.76+86_76+101delinsTCATATTTTGAAATTC
NM_006567.5:c.772+86_772+101delinsTCATATTTTGAAATTC MANE Select	NP_006558.1:n.772+86_772+101delinsTCATATTTTGAAATTC