Canonical Allele Identifier: CA2769854404

Gene: FARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.5613412_5613413insACA , CM000668.2:g.5613412_5613413insACA	GRCh38
NC_000006.11:g.5613645_5613646insACA , CM000668.1:g.5613645_5613646insACA	GRCh37
NC_000006.10:g.5558644_5558645insACA	NCBI36
NG_033003.1:g.357062_357063insACA
NG_033003.2:g.357062_357063insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274680.9:c.1217+92_1217+93insACA MANE Select	ENSP00000274680.4:n.1217+92_1217+93insACA
ENST00000648580.1:c.1217+92_1217+93insACA	ENSP00000497889.1:n.1217+92_1217+93insACA
ENST00000274680.8:c.1217+92_1217+93insACA	ENSP00000274680.3:n.1217+92_1217+93insACA
ENST00000324331.10:c.1217+92_1217+93insACA	ENSP00000316335.5:n.1217+92_1217+93insACA
NM_006567.3:c.1217+92_1217+93insACA	NP_006558.1:n.1217+92_1217+93insACA
XM_005248811.1:c.1217+92_1217+93insACA	XP_005248868.1:n.1217+92_1217+93insACA
XM_005248812.2:c.1217+92_1217+93insACA	XP_005248869.1:n.1217+92_1217+93insACA
XM_011514247.1:c.1217+92_1217+93insACA	XP_011512549.1:n.1217+92_1217+93insACA
XM_011514248.1:c.1217+92_1217+93insACA	XP_011512550.1:n.1217+92_1217+93insACA
XM_011514249.1:c.1217+92_1217+93insACA	XP_011512551.1:n.1217+92_1217+93insACA
XR_926026.1:n.2191+92_2191+93insACA
XR_926028.1:n.1680+92_1680+93insACA
NM_001318872.1:c.1217+92_1217+93insACA	NP_001305801.1:n.1217+92_1217+93insACA
NM_006567.4:c.1217+92_1217+93insACA	NP_006558.1:n.1217+92_1217+93insACA
XM_005248812.3:c.1217+92_1217+93insACA	XP_005248869.1:n.1217+92_1217+93insACA
XM_011514247.3:c.1217+92_1217+93insACA	XP_011512549.1:n.1217+92_1217+93insACA
XM_011514248.3:c.1217+92_1217+93insACA	XP_011512550.1:n.1217+92_1217+93insACA
XM_011514249.2:c.1217+92_1217+93insACA	XP_011512551.1:n.1217+92_1217+93insACA
XM_017010186.1:c.1217+92_1217+93insACA	XP_016865675.1:n.1217+92_1217+93insACA
XM_017010187.1:c.1217+92_1217+93insACA	XP_016865676.1:n.1217+92_1217+93insACA
XR_926028.2:n.1657+92_1657+93insACA
NM_001318872.2:c.1217+92_1217+93insACA	NP_001305801.1:n.1217+92_1217+93insACA
NM_001374875.1:c.1217+92_1217+93insACA	NP_001361804.1:n.1217+92_1217+93insACA
NM_001374876.1:c.1217+92_1217+93insACA	NP_001361805.1:n.1217+92_1217+93insACA
NM_001374877.1:c.1217+92_1217+93insACA	NP_001361806.1:n.1217+92_1217+93insACA
NM_001374878.1:c.1217+92_1217+93insACA	NP_001361807.1:n.1217+92_1217+93insACA
NM_001374879.1:c.1217+92_1217+93insACA	NP_001361808.1:n.1217+92_1217+93insACA
NM_001375257.1:c.1217+92_1217+93insACA	NP_001362186.1:n.1217+92_1217+93insACA
NM_001375258.1:c.1085+92_1085+93insACA	NP_001362187.1:n.1085+92_1085+93insACA
NM_001375259.1:c.521+92_521+93insACA	NP_001362188.1:n.521+92_521+93insACA
NM_001375260.1:c.521+92_521+93insACA	NP_001362189.1:n.521+92_521+93insACA
NM_006567.5:c.1217+92_1217+93insACA MANE Select	NP_006558.1:n.1217+92_1217+93insACA