Canonical Allele Identifier: CA2612565766
Gene: FAR1 HGNC NCBI

Linked Data

gnomAD v4: 11-13728584-C-CT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728585dup , CM000673.2:g.13728585dup GRCh38
NC_000011.9:g.13750132dup , CM000673.1:g.13750132dup GRCh37
NC_000011.8:g.13706708dup NCBI36
NG_041826.1:g.64927dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000703358.1:c.*211-27dup ENSP00000515269.1:n.*211-27dup
ENST00000354817.8:c.1386-27dup MANE Select ENSP00000346874.3:n.1386-27dup
ENST00000354817.7:c.1386-27dup ENSP00000346874.3:n.1386-27dup
ENST00000532502.1:c.258-27dup ENSP00000434624.1:n.258-27dup
NM_032228.5:c.1386-27dup NP_115604.1:n.1386-27dup
XM_011520400.1:c.1395-27dup XP_011518702.1:n.1395-27dup
XM_011520401.1:c.1218-27dup XP_011518703.1:n.1218-27dup
XM_011520400.2:c.1395-27dup XP_011518702.1:n.1395-27dup
NM_032228.6:c.1386-27dup MANE Select NP_115604.1:n.1386-27dup
Search 100 bp 5'
Search 100 bp 3'