Canonical Allele Identifier: CA473229144
Gene: FAR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.13750216T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13728669T>A , CM000673.2:g.13728669T>A GRCh38
NC_000011.9:g.13750216T>A , CM000673.1:g.13750216T>A GRCh37
NC_000011.8:g.13706792T>A NCBI36
NG_041826.1:g.65011T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703358.1:c.*268T>A ENSP00000515269.1:n.*268T>A
ENST00000354817.8:c.1443T>A MANE Select ENSP00000346874.3:p.Ile481=
ENST00000354817.7:c.1443T>A ENSP00000346874.3:p.Ile481=
ENST00000532502.1:c.315T>A ENSP00000434624.1:p.Ile105=
NM_032228.5:c.1443T>A NP_115604.1:p.Ile481=
XM_011520400.1:c.1452T>A XP_011518702.1:p.Ile484=
XM_011520401.1:c.1275T>A XP_011518703.1:p.Ile425=
XM_011520400.2:c.1452T>A XP_011518702.1:p.Ile484=
NM_032228.6:c.1443T>A MANE Select NP_115604.1:p.Ile481=