Canonical Allele Identifier: CA379859384

Gene: FAR1

Linked Data

• MyVariant Identifiers: chr11:g.13750217T>C (hg19) ; chr11:g.13728670T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13728670T>C , CM000673.2:g.13728670T>C	GRCh38
NC_000011.9:g.13750217T>C , CM000673.1:g.13750217T>C	GRCh37
NC_000011.8:g.13706793T>C	NCBI36
NG_041826.1:g.65012T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703358.1:c.*269T>C	ENSP00000515269.1:n.*269T>C
ENST00000354817.8:c.1444T>C MANE Select	ENSP00000346874.3:p.Phe482Leu
ENST00000354817.7:c.1444T>C	ENSP00000346874.3:p.Phe482Leu
ENST00000532502.1:c.316T>C	ENSP00000434624.1:p.Phe106Leu
NM_032228.5:c.1444T>C	NP_115604.1:p.Phe482Leu
XM_011520400.1:c.1453T>C	XP_011518702.1:p.Phe485Leu
XM_011520401.1:c.1276T>C	XP_011518703.1:p.Phe426Leu
XM_011520400.2:c.1453T>C	XP_011518702.1:p.Phe485Leu
NM_032228.6:c.1444T>C MANE Select	NP_115604.1:p.Phe482Leu