Canonical Allele Identifier: CA3623838

Gene: FARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.5545200G>C , CM000668.2:g.5545200G>C	GRCh38
NC_000006.11:g.5545433G>C , CM000668.1:g.5545433G>C	GRCh37
NC_000006.10:g.5490432G>C	NCBI36
NG_033003.1:g.288850G>C
NG_033003.2:g.288850G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_006567.5:c.925G>C MANE Select	NP_006558.1:p.Gly309Arg
ENST00000274680.9:c.925G>C MANE Select	ENSP00000274680.4:p.Gly309Arg
NM_001318872.1:c.925G>C	NP_001305801.1:p.Gly309Arg
NM_001318872.2:c.925G>C	NP_001305801.1:p.Gly309Arg
NM_001374875.1:c.925G>C	NP_001361804.1:p.Gly309Arg
NM_001374876.1:c.925G>C	NP_001361805.1:p.Gly309Arg
NM_001374877.1:c.925G>C	NP_001361806.1:p.Gly309Arg
NM_001374878.1:c.925G>C	NP_001361807.1:p.Gly309Arg
NM_001374879.1:c.925G>C	NP_001361808.1:p.Gly309Arg
NM_001375257.1:c.925G>C	NP_001362186.1:p.Gly309Arg
NM_001375258.1:c.793G>C	NP_001362187.1:p.Gly265Arg
NM_001375259.1:c.229G>C	NP_001362188.1:p.Gly77Arg
NM_001375260.1:c.229G>C	NP_001362189.1:p.Gly77Arg
NM_006567.3:c.925G>C	NP_006558.1:p.Gly309Arg
NM_006567.4:c.925G>C	NP_006558.1:p.Gly309Arg
ENST00000274680.8:c.925G>C	ENSP00000274680.3:p.Gly309Arg
ENST00000324331.10:c.925G>C	ENSP00000316335.5:p.Gly309Arg
ENST00000648580.1:c.925G>C	ENSP00000497889.1:p.Gly309Arg
XM_005248811.1:c.925G>C	XP_005248868.1:p.Gly309Arg
XM_005248812.2:c.925G>C	XP_005248869.1:p.Gly309Arg
XM_005248812.3:c.925G>C	XP_005248869.1:p.Gly309Arg
XM_011514247.1:c.925G>C	XP_011512549.1:p.Gly309Arg
XM_011514247.3:c.925G>C	XP_011512549.1:p.Gly309Arg
XM_011514248.1:c.925G>C	XP_011512550.1:p.Gly309Arg
XM_011514248.3:c.925G>C	XP_011512550.1:p.Gly309Arg
XM_011514249.1:c.925G>C	XP_011512551.1:p.Gly309Arg
XM_011514249.2:c.925G>C	XP_011512551.1:p.Gly309Arg
XM_017010186.1:c.925G>C	XP_016865675.1:p.Gly309Arg
XM_017010187.1:c.925G>C	XP_016865676.1:p.Gly309Arg
XR_926026.1:n.1899G>C
XR_926027.1:n.1767G>C
XR_926027.3:n.1744G>C
XR_926028.1:n.1388G>C
XR_926028.2:n.1365G>C