Canonical Allele Identifier: CA473229141
Gene: FAR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.13750213C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728666C>A , CM000673.2:g.13728666C>A GRCh38
NC_000011.9:g.13750213C>A , CM000673.1:g.13750213C>A GRCh37
NC_000011.8:g.13706789C>A NCBI36
NG_041826.1:g.65008C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703358.1:c.*265C>A ENSP00000515269.1:n.*265C>A
ENST00000354817.8:c.1440C>A MANE Select ENSP00000346874.3:p.Arg480=
ENST00000354817.7:c.1440C>A ENSP00000346874.3:p.Arg480=
ENST00000532502.1:c.312C>A ENSP00000434624.1:p.Arg104=
NM_032228.5:c.1440C>A NP_115604.1:p.Arg480=
XM_011520400.1:c.1449C>A XP_011518702.1:p.Arg483=
XM_011520401.1:c.1272C>A XP_011518703.1:p.Arg424=
XM_011520400.2:c.1449C>A XP_011518702.1:p.Arg483=
NM_032228.6:c.1440C>A MANE Select NP_115604.1:p.Arg480=