Canonical Allele Identifier: CA1607612124

Gene: FARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.5404768_5404769delinsTG , CM000668.2:g.5404768_5404769delinsTG	GRCh38
NC_000006.11:g.5405001_5405002delinsTG , CM000668.1:g.5405001_5405002delinsTG	GRCh37
NC_000006.10:g.5350000_5350001delinsTG	NCBI36
NG_033003.1:g.148418_148419delinsTG
NG_033003.2:g.148418_148419delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274680.9:c.772+67_772+68delinsTG MANE Select	ENSP00000274680.4:n.772+67_772+68delinsTG
ENST00000648580.1:c.772+67_772+68delinsTG	ENSP00000497889.1:n.772+67_772+68delinsTG
ENST00000274680.8:c.772+67_772+68delinsTG	ENSP00000274680.3:n.772+67_772+68delinsTG
ENST00000324331.10:c.772+67_772+68delinsTG	ENSP00000316335.5:n.772+67_772+68delinsTG
ENST00000445533.1:c.160+67_160+68delinsTG	ENSP00000392525.1:n.160+67_160+68delinsTG
NM_006567.3:c.772+67_772+68delinsTG	NP_006558.1:n.772+67_772+68delinsTG
XM_005248811.1:c.772+67_772+68delinsTG	XP_005248868.1:n.772+67_772+68delinsTG
XM_005248812.2:c.772+67_772+68delinsTG	XP_005248869.1:n.772+67_772+68delinsTG
XM_006714966.1:c.772+67_772+68delinsTG	XP_006715029.1:n.772+67_772+68delinsTG
XM_011514247.1:c.772+67_772+68delinsTG	XP_011512549.1:n.772+67_772+68delinsTG
XM_011514248.1:c.772+67_772+68delinsTG	XP_011512550.1:n.772+67_772+68delinsTG
XM_011514249.1:c.772+67_772+68delinsTG	XP_011512551.1:n.772+67_772+68delinsTG
XM_011514250.1:c.772+67_772+68delinsTG	XP_011512552.1:n.772+67_772+68delinsTG
XM_011514251.1:c.772+67_772+68delinsTG	XP_011512553.1:n.772+67_772+68delinsTG
XR_926026.1:n.1103+67_1103+68delinsTG
XR_926027.1:n.1103+67_1103+68delinsTG
XR_926028.1:n.1103+67_1103+68delinsTG
NM_001318872.1:c.772+67_772+68delinsTG	NP_001305801.1:n.772+67_772+68delinsTG
NM_006567.4:c.772+67_772+68delinsTG	NP_006558.1:n.772+67_772+68delinsTG
XM_005248812.3:c.772+67_772+68delinsTG	XP_005248869.1:n.772+67_772+68delinsTG
XM_006714966.3:c.772+67_772+68delinsTG	XP_006715029.1:n.772+67_772+68delinsTG
XM_011514247.3:c.772+67_772+68delinsTG	XP_011512549.1:n.772+67_772+68delinsTG
XM_011514248.3:c.772+67_772+68delinsTG	XP_011512550.1:n.772+67_772+68delinsTG
XM_011514249.2:c.772+67_772+68delinsTG	XP_011512551.1:n.772+67_772+68delinsTG
XM_011514251.3:c.772+67_772+68delinsTG	XP_011512553.1:n.772+67_772+68delinsTG
XM_017010186.1:c.772+67_772+68delinsTG	XP_016865675.1:n.772+67_772+68delinsTG
XM_017010187.1:c.772+67_772+68delinsTG	XP_016865676.1:n.772+67_772+68delinsTG
XR_926027.3:n.1080+67_1080+68delinsTG
XR_926028.2:n.1080+67_1080+68delinsTG
NM_001318872.2:c.772+67_772+68delinsTG	NP_001305801.1:n.772+67_772+68delinsTG
NM_001374875.1:c.772+67_772+68delinsTG	NP_001361804.1:n.772+67_772+68delinsTG
NM_001374876.1:c.772+67_772+68delinsTG	NP_001361805.1:n.772+67_772+68delinsTG
NM_001374877.1:c.772+67_772+68delinsTG	NP_001361806.1:n.772+67_772+68delinsTG
NM_001374878.1:c.772+67_772+68delinsTG	NP_001361807.1:n.772+67_772+68delinsTG
NM_001374879.1:c.772+67_772+68delinsTG	NP_001361808.1:n.772+67_772+68delinsTG
NM_001375257.1:c.772+67_772+68delinsTG	NP_001362186.1:n.772+67_772+68delinsTG
NM_001375258.1:c.772+67_772+68delinsTG	NP_001362187.1:n.772+67_772+68delinsTG
NM_001375259.1:c.76+67_76+68delinsTG	NP_001362188.1:n.76+67_76+68delinsTG
NM_001375260.1:c.76+67_76+68delinsTG	NP_001362189.1:n.76+67_76+68delinsTG
NM_006567.5:c.772+67_772+68delinsTG MANE Select	NP_006558.1:n.772+67_772+68delinsTG