Canonical Allele Identifier: CA2612565768
Gene: FAR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728587A>G , CM000673.2:g.13728587A>G GRCh38
NC_000011.9:g.13750134A>G , CM000673.1:g.13750134A>G GRCh37
NC_000011.8:g.13706710A>G NCBI36
NG_041826.1:g.64929A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703358.1:c.*211-25A>G ENSP00000515269.1:n.*211-25A>G
ENST00000354817.8:c.1386-25A>G MANE Select ENSP00000346874.3:n.1386-25A>G
ENST00000354817.7:c.1386-25A>G ENSP00000346874.3:n.1386-25A>G
ENST00000532502.1:c.258-25A>G ENSP00000434624.1:n.258-25A>G
NM_032228.5:c.1386-25A>G NP_115604.1:n.1386-25A>G
XM_011520400.1:c.1395-25A>G XP_011518702.1:n.1395-25A>G
XM_011520401.1:c.1218-25A>G XP_011518703.1:n.1218-25A>G
XM_011520400.2:c.1395-25A>G XP_011518702.1:n.1395-25A>G
NM_032228.6:c.1386-25A>G MANE Select NP_115604.1:n.1386-25A>G