Canonical Allele Identifier: CA2540293639
Gene: FAR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728584_13728585insCAA , CM000673.2:g.13728584_13728585insCAA GRCh38
NC_000011.9:g.13750131_13750132insCAA , CM000673.1:g.13750131_13750132insCAA GRCh37
NC_000011.8:g.13706707_13706708insCAA NCBI36
NG_041826.1:g.64926_64927insCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000703358.1:c.*211-28_*211-27insCAA ENSP00000515269.1:n.*211-28_*211-27insCAA
ENST00000354817.8:c.1386-28_1386-27insCAA MANE Select ENSP00000346874.3:n.1386-28_1386-27insCAA
ENST00000354817.7:c.1386-28_1386-27insCAA ENSP00000346874.3:n.1386-28_1386-27insCAA
ENST00000532502.1:c.258-28_258-27insCAA ENSP00000434624.1:n.258-28_258-27insCAA
NM_032228.5:c.1386-28_1386-27insCAA NP_115604.1:n.1386-28_1386-27insCAA
XM_011520400.1:c.1395-28_1395-27insCAA XP_011518702.1:n.1395-28_1395-27insCAA
XM_011520401.1:c.1218-28_1218-27insCAA XP_011518703.1:n.1218-28_1218-27insCAA
XM_011520400.2:c.1395-28_1395-27insCAA XP_011518702.1:n.1395-28_1395-27insCAA
NM_032228.6:c.1386-28_1386-27insCAA MANE Select NP_115604.1:n.1386-28_1386-27insCAA
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