Canonical Allele Identifier: CA1953439103
Gene: FAR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728665G= , CM000673.2:g.13728665G= GRCh38
NC_000011.9:g.13750212G= , CM000673.1:g.13750212G= GRCh37
NC_000011.8:g.13706788G= NCBI36
NG_041826.1:g.65007G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703358.1:c.*264G= ENSP00000515269.1:n.*264G=
ENST00000354817.8:c.1439G= MANE Select ENSP00000346874.3:p.Arg480=
ENST00000354817.7:c.1439G= ENSP00000346874.3:p.Arg480=
ENST00000532502.1:c.311G= ENSP00000434624.1:p.Arg104=
NM_032228.5:c.1439G= NP_115604.1:p.Arg480=
XM_011520400.1:c.1448G= XP_011518702.1:p.Arg483=
XM_011520401.1:c.1271G= XP_011518703.1:p.Arg424=
XM_011520400.2:c.1448G= XP_011518702.1:p.Arg483=
NM_032228.6:c.1439G= MANE Select NP_115604.1:p.Arg480=