Canonical Allele Identifier: CA134301674

Gene: FARS2

Linked Data

• dbSNP Id: rs150294010
• gnomAD v2: 6-5369551-AATGAC-A
• gnomAD v3: 6-5369318-AATGAC-A
• gnomAD v4: 6-5369318-AATGAC-A
• MyVariant Identifiers: chr6:g.5369552_5369556del (hg19) ; chr6:g.5369319_5369323del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.5369321_5369325del , CM000668.2:g.5369321_5369325del	GRCh38
NC_000006.11:g.5369554_5369558del , CM000668.1:g.5369554_5369558del	GRCh37
NC_000006.10:g.5314553_5314557del	NCBI36
NG_033003.1:g.112971_112975del
NG_033003.2:g.112971_112975del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274680.9:c.612+139_612+143del MANE Select	ENSP00000274680.4:n.612+139_612+143del
ENST00000648580.1:c.612+139_612+143del	ENSP00000497889.1:n.612+139_612+143del
ENST00000274680.8:c.612+139_612+143del	ENSP00000274680.3:n.612+139_612+143del
ENST00000324331.10:c.612+139_612+143del	ENSP00000316335.5:n.612+139_612+143del
NM_006567.3:c.612+139_612+143del	NP_006558.1:n.612+139_612+143del
XM_005248811.1:c.612+139_612+143del	XP_005248868.1:n.612+139_612+143del
XM_005248812.2:c.612+139_612+143del	XP_005248869.1:n.612+139_612+143del
XM_006714966.1:c.612+139_612+143del	XP_006715029.1:n.612+139_612+143del
XM_011514247.1:c.612+139_612+143del	XP_011512549.1:n.612+139_612+143del
XM_011514248.1:c.612+139_612+143del	XP_011512550.1:n.612+139_612+143del
XM_011514249.1:c.612+139_612+143del	XP_011512551.1:n.612+139_612+143del
XM_011514250.1:c.612+139_612+143del	XP_011512552.1:n.612+139_612+143del
XM_011514251.1:c.612+139_612+143del	XP_011512553.1:n.612+139_612+143del
XR_926026.1:n.943+139_943+143del
XR_926027.1:n.943+139_943+143del
XR_926028.1:n.943+139_943+143del
NM_001318872.1:c.612+139_612+143del	NP_001305801.1:n.612+139_612+143del
NM_006567.4:c.612+139_612+143del	NP_006558.1:n.612+139_612+143del
XM_005248812.3:c.612+139_612+143del	XP_005248869.1:n.612+139_612+143del
XM_006714966.3:c.612+139_612+143del	XP_006715029.1:n.612+139_612+143del
XM_011514247.3:c.612+139_612+143del	XP_011512549.1:n.612+139_612+143del
XM_011514248.3:c.612+139_612+143del	XP_011512550.1:n.612+139_612+143del
XM_011514249.2:c.612+139_612+143del	XP_011512551.1:n.612+139_612+143del
XM_011514251.3:c.612+139_612+143del	XP_011512553.1:n.612+139_612+143del
XM_017010186.1:c.612+139_612+143del	XP_016865675.1:n.612+139_612+143del
XM_017010187.1:c.612+139_612+143del	XP_016865676.1:n.612+139_612+143del
XR_926027.3:n.920+139_920+143del
XR_926028.2:n.920+139_920+143del
NM_001318872.2:c.612+139_612+143del	NP_001305801.1:n.612+139_612+143del
NM_001374875.1:c.612+139_612+143del	NP_001361804.1:n.612+139_612+143del
NM_001374876.1:c.612+139_612+143del	NP_001361805.1:n.612+139_612+143del
NM_001374877.1:c.612+139_612+143del	NP_001361806.1:n.612+139_612+143del
NM_001374878.1:c.612+139_612+143del	NP_001361807.1:n.612+139_612+143del
NM_001374879.1:c.612+139_612+143del	NP_001361808.1:n.612+139_612+143del
NM_001375257.1:c.612+139_612+143del	NP_001362186.1:n.612+139_612+143del
NM_001375258.1:c.612+139_612+143del	NP_001362187.1:n.612+139_612+143del
NM_001375259.1:c.-84-35221_-84-35217del	NP_001362188.1:n.-84-35221_-84-35217del
NM_001375260.1:c.-340-27312_-340-27308del	NP_001362189.1:n.-340-27312_-340-27308del
NM_006567.5:c.612+139_612+143del MANE Select	NP_006558.1:n.612+139_612+143del