Canonical Allele Identifier: CA1607705365
Gene: FARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.5613270_5613276delinsAGGAGAC , CM000668.2:g.5613270_5613276delinsAGGAGAC GRCh38
NC_000006.11:g.5613503_5613509delinsAGGAGAC , CM000668.1:g.5613503_5613509delinsAGGAGAC GRCh37
NC_000006.10:g.5558502_5558508delinsAGGAGAC NCBI36
NG_033003.1:g.356920_356926delinsAGGAGAC
NG_033003.2:g.356920_356926delinsAGGAGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000274680.9:c.1167_1173delinsAGGAGAC MANE Select ENSP00000274680.4:p.Gly389=
ENST00000648580.1:c.1167_1173delinsAGGAGAC ENSP00000497889.1:p.Gly389=
ENST00000274680.8:c.1167_1173delinsAGGAGAC ENSP00000274680.3:p.Gly389=
ENST00000324331.10:c.1167_1173delinsAGGAGAC ENSP00000316335.5:p.Gly389=
NM_006567.3:c.1167_1173delinsAGGAGAC NP_006558.1:p.Gly389=
XM_005248811.1:c.1167_1173delinsAGGAGAC XP_005248868.1:p.Gly389=
XM_005248812.2:c.1167_1173delinsAGGAGAC XP_005248869.1:p.Gly389=
XM_011514247.1:c.1167_1173delinsAGGAGAC XP_011512549.1:p.Gly389=
XM_011514248.1:c.1167_1173delinsAGGAGAC XP_011512550.1:p.Gly389=
XM_011514249.1:c.1167_1173delinsAGGAGAC XP_011512551.1:p.Gly389=
XR_926026.1:n.2141_2147delinsAGGAGAC
XR_926028.1:n.1630_1636delinsAGGAGAC
NM_001318872.1:c.1167_1173delinsAGGAGAC NP_001305801.1:p.Gly389=
NM_006567.4:c.1167_1173delinsAGGAGAC NP_006558.1:p.Gly389=
XM_005248812.3:c.1167_1173delinsAGGAGAC XP_005248869.1:p.Gly389=
XM_011514247.3:c.1167_1173delinsAGGAGAC XP_011512549.1:p.Gly389=
XM_011514248.3:c.1167_1173delinsAGGAGAC XP_011512550.1:p.Gly389=
XM_011514249.2:c.1167_1173delinsAGGAGAC XP_011512551.1:p.Gly389=
XM_017010186.1:c.1167_1173delinsAGGAGAC XP_016865675.1:p.Gly389=
XM_017010187.1:c.1167_1173delinsAGGAGAC XP_016865676.1:p.Gly389=
XR_926028.2:n.1607_1613delinsAGGAGAC
NM_001318872.2:c.1167_1173delinsAGGAGAC NP_001305801.1:p.Gly389=
NM_001374875.1:c.1167_1173delinsAGGAGAC NP_001361804.1:p.Gly389=
NM_001374876.1:c.1167_1173delinsAGGAGAC NP_001361805.1:p.Gly389=
NM_001374877.1:c.1167_1173delinsAGGAGAC NP_001361806.1:p.Gly389=
NM_001374878.1:c.1167_1173delinsAGGAGAC NP_001361807.1:p.Gly389=
NM_001374879.1:c.1167_1173delinsAGGAGAC NP_001361808.1:p.Gly389=
NM_001375257.1:c.1167_1173delinsAGGAGAC NP_001362186.1:p.Gly389=
NM_001375258.1:c.1035_1041delinsAGGAGAC NP_001362187.1:p.Gly345=
NM_001375259.1:c.471_477delinsAGGAGAC NP_001362188.1:p.Gly157=
NM_001375260.1:c.471_477delinsAGGAGAC NP_001362189.1:p.Gly157=
NM_006567.5:c.1167_1173delinsAGGAGAC MANE Select NP_006558.1:p.Gly389=