Canonical Allele Identifier: CA2612565751
Gene: FAR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728569del , CM000673.2:g.13728569del GRCh38
NC_000011.9:g.13750116del , CM000673.1:g.13750116del GRCh37
NC_000011.8:g.13706692del NCBI36
NG_041826.1:g.64911del

Transcript Alleles

HGVS Amino-acid change
ENST00000703358.1:c.*211-43del ENSP00000515269.1:n.*211-43del
ENST00000354817.8:c.1386-43del MANE Select ENSP00000346874.3:n.1386-43del
ENST00000354817.7:c.1386-43del ENSP00000346874.3:n.1386-43del
ENST00000532502.1:c.258-43del ENSP00000434624.1:n.258-43del
NM_032228.5:c.1386-43del NP_115604.1:n.1386-43del
XM_011520400.1:c.1395-43del XP_011518702.1:n.1395-43del
XM_011520401.1:c.1218-43del XP_011518703.1:n.1218-43del
XM_011520400.2:c.1395-43del XP_011518702.1:n.1395-43del
NM_032228.6:c.1386-43del MANE Select NP_115604.1:n.1386-43del