Canonical Allele Identifier: CA448634141

Gene: FARS2

Linked Data

• MyVariant Identifiers: chr6:g.5613551A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.5613318A>C , CM000668.2:g.5613318A>C	GRCh38
NC_000006.11:g.5613551A>C , CM000668.1:g.5613551A>C	GRCh37
NC_000006.10:g.5558550A>C	NCBI36
NG_033003.1:g.356968A>C
NG_033003.2:g.356968A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274680.9:c.1215A>C MANE Select	ENSP00000274680.4:p.Pro405=
ENST00000648580.1:c.1215A>C	ENSP00000497889.1:p.Pro405=
ENST00000274680.8:c.1215A>C	ENSP00000274680.3:p.Pro405=
ENST00000324331.10:c.1215A>C	ENSP00000316335.5:p.Pro405=
NM_006567.3:c.1215A>C	NP_006558.1:p.Pro405=
XM_005248811.1:c.1215A>C	XP_005248868.1:p.Pro405=
XM_005248812.2:c.1215A>C	XP_005248869.1:p.Pro405=
XM_011514247.1:c.1215A>C	XP_011512549.1:p.Pro405=
XM_011514248.1:c.1215A>C	XP_011512550.1:p.Pro405=
XM_011514249.1:c.1215A>C	XP_011512551.1:p.Pro405=
XR_926026.1:n.2189A>C
XR_926028.1:n.1678A>C
NM_001318872.1:c.1215A>C	NP_001305801.1:p.Pro405=
NM_006567.4:c.1215A>C	NP_006558.1:p.Pro405=
XM_005248812.3:c.1215A>C	XP_005248869.1:p.Pro405=
XM_011514247.3:c.1215A>C	XP_011512549.1:p.Pro405=
XM_011514248.3:c.1215A>C	XP_011512550.1:p.Pro405=
XM_011514249.2:c.1215A>C	XP_011512551.1:p.Pro405=
XM_017010186.1:c.1215A>C	XP_016865675.1:p.Pro405=
XM_017010187.1:c.1215A>C	XP_016865676.1:p.Pro405=
XR_926028.2:n.1655A>C
NM_001318872.2:c.1215A>C	NP_001305801.1:p.Pro405=
NM_001374875.1:c.1215A>C	NP_001361804.1:p.Pro405=
NM_001374876.1:c.1215A>C	NP_001361805.1:p.Pro405=
NM_001374877.1:c.1215A>C	NP_001361806.1:p.Pro405=
NM_001374878.1:c.1215A>C	NP_001361807.1:p.Pro405=
NM_001374879.1:c.1215A>C	NP_001361808.1:p.Pro405=
NM_001375257.1:c.1215A>C	NP_001362186.1:p.Pro405=
NM_001375258.1:c.1083A>C	NP_001362187.1:p.Pro361=
NM_001375259.1:c.519A>C	NP_001362188.1:p.Pro173=
NM_001375260.1:c.519A>C	NP_001362189.1:p.Pro173=
NM_006567.5:c.1215A>C MANE Select	NP_006558.1:p.Pro405=