Canonical Allele Identifier: CA473229146

Gene: FAR1

Linked Data

• MyVariant Identifiers: chr11:g.13750219T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13728672T>C , CM000673.2:g.13728672T>C	GRCh38
NC_000011.9:g.13750219T>C , CM000673.1:g.13750219T>C	GRCh37
NC_000011.8:g.13706795T>C	NCBI36
NG_041826.1:g.65014T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703358.1:c.*271T>C	ENSP00000515269.1:n.*271T>C
ENST00000354817.8:c.1446T>C MANE Select	ENSP00000346874.3:p.Phe482=
ENST00000354817.7:c.1446T>C	ENSP00000346874.3:p.Phe482=
ENST00000532502.1:c.318T>C	ENSP00000434624.1:p.Phe106=
NM_032228.5:c.1446T>C	NP_115604.1:p.Phe482=
XM_011520400.1:c.1455T>C	XP_011518702.1:p.Phe485=
XM_011520401.1:c.1278T>C	XP_011518703.1:p.Phe426=
XM_011520400.2:c.1455T>C	XP_011518702.1:p.Phe485=
NM_032228.6:c.1446T>C MANE Select	NP_115604.1:p.Phe482=