Canonical Allele Identifier: CA1953439075
Gene: FAR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728589A= , CM000673.2:g.13728589A= GRCh38
NC_000011.9:g.13750136A= , CM000673.1:g.13750136A= GRCh37
NC_000011.8:g.13706712A= NCBI36
NG_041826.1:g.64931A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703358.1:c.*211-23A= ENSP00000515269.1:n.*211-23A=
ENST00000354817.8:c.1386-23A= MANE Select ENSP00000346874.3:n.1386-23A=
ENST00000354817.7:c.1386-23A= ENSP00000346874.3:n.1386-23A=
ENST00000532502.1:c.258-23A= ENSP00000434624.1:n.258-23A=
NM_032228.5:c.1386-23A= NP_115604.1:n.1386-23A=
XM_011520400.1:c.1395-23A= XP_011518702.1:n.1395-23A=
XM_011520401.1:c.1218-23A= XP_011518703.1:n.1218-23A=
XM_011520400.2:c.1395-23A= XP_011518702.1:n.1395-23A=
NM_032228.6:c.1386-23A= MANE Select NP_115604.1:n.1386-23A=