Canonical Allele Identifier: CA379859382
Gene: FAR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728670T>G , CM000673.2:g.13728670T>G GRCh38
NC_000011.9:g.13750217T>G , CM000673.1:g.13750217T>G GRCh37
NC_000011.8:g.13706793T>G NCBI36
NG_041826.1:g.65012T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703358.1:c.*269T>G ENSP00000515269.1:n.*269T>G
ENST00000354817.8:c.1444T>G MANE Select ENSP00000346874.3:p.Phe482Val
ENST00000354817.7:c.1444T>G ENSP00000346874.3:p.Phe482Val
ENST00000532502.1:c.316T>G ENSP00000434624.1:p.Phe106Val
NM_032228.5:c.1444T>G NP_115604.1:p.Phe482Val
XM_011520400.1:c.1453T>G XP_011518702.1:p.Phe485Val
XM_011520401.1:c.1276T>G XP_011518703.1:p.Phe426Val
XM_011520400.2:c.1453T>G XP_011518702.1:p.Phe485Val
NM_032228.6:c.1444T>G MANE Select NP_115604.1:p.Phe482Val