Canonical Allele Identifier: CA325392
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214335
dbSNP Id: rs751459058
gnomAD v2: 6-5613418-C-T
gnomAD v3: 6-5613185-C-T
gnomAD v4: 6-5613185-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.5613185C>T , CM000668.2:g.5613185C>T GRCh38
NC_000006.11:g.5613418C>T , CM000668.1:g.5613418C>T GRCh37
NC_000006.10:g.5558417C>T NCBI36
NG_033003.1:g.356835C>T
NG_033003.2:g.356835C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274680.9:c.1082C>T MANE Select ENSP00000274680.4:p.Pro361Leu
ENST00000648580.1:c.1082C>T ENSP00000497889.1:p.Pro361Leu
ENST00000274680.8:c.1082C>T ENSP00000274680.3:p.Pro361Leu
ENST00000324331.10:c.1082C>T ENSP00000316335.5:p.Pro361Leu
NM_006567.3:c.1082C>T NP_006558.1:p.Pro361Leu
XM_005248811.1:c.1082C>T XP_005248868.1:p.Pro361Leu
XM_005248812.2:c.1082C>T XP_005248869.1:p.Pro361Leu
XM_011514247.1:c.1082C>T XP_011512549.1:p.Pro361Leu
XM_011514248.1:c.1082C>T XP_011512550.1:p.Pro361Leu
XM_011514249.1:c.1082C>T XP_011512551.1:p.Pro361Leu
XR_926026.1:n.2056C>T
XR_926028.1:n.1545C>T
NM_001318872.1:c.1082C>T NP_001305801.1:p.Pro361Leu
NM_006567.4:c.1082C>T NP_006558.1:p.Pro361Leu
XM_005248812.3:c.1082C>T XP_005248869.1:p.Pro361Leu
XM_011514247.3:c.1082C>T XP_011512549.1:p.Pro361Leu
XM_011514248.3:c.1082C>T XP_011512550.1:p.Pro361Leu
XM_011514249.2:c.1082C>T XP_011512551.1:p.Pro361Leu
XM_017010186.1:c.1082C>T XP_016865675.1:p.Pro361Leu
XM_017010187.1:c.1082C>T XP_016865676.1:p.Pro361Leu
XR_926028.2:n.1522C>T
NM_001318872.2:c.1082C>T NP_001305801.1:p.Pro361Leu
NM_001374875.1:c.1082C>T NP_001361804.1:p.Pro361Leu
NM_001374876.1:c.1082C>T NP_001361805.1:p.Pro361Leu
NM_001374877.1:c.1082C>T NP_001361806.1:p.Pro361Leu
NM_001374878.1:c.1082C>T NP_001361807.1:p.Pro361Leu
NM_001374879.1:c.1082C>T NP_001361808.1:p.Pro361Leu
NM_001375257.1:c.1082C>T NP_001362186.1:p.Pro361Leu
NM_001375258.1:c.950C>T NP_001362187.1:p.Pro317Leu
NM_001375259.1:c.386C>T NP_001362188.1:p.Pro129Leu
NM_001375260.1:c.386C>T NP_001362189.1:p.Pro129Leu
NM_006567.5:c.1082C>T MANE Select NP_006558.1:p.Pro361Leu