Canonical Allele Identifier: CA473229152

Gene: FAR1

Linked Data

• MyVariant Identifiers: chr11:g.13750225A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13728678A>T , CM000673.2:g.13728678A>T	GRCh38
NC_000011.9:g.13750225A>T , CM000673.1:g.13750225A>T	GRCh37
NC_000011.8:g.13706801A>T	NCBI36
NG_041826.1:g.65020A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703358.1:c.*277A>T	ENSP00000515269.1:n.*277A>T
ENST00000354817.8:c.1452A>T MANE Select	ENSP00000346874.3:p.Ala484=
ENST00000354817.7:c.1452A>T	ENSP00000346874.3:p.Ala484=
ENST00000532502.1:c.324A>T	ENSP00000434624.1:p.Ala108=
NM_032228.5:c.1452A>T	NP_115604.1:p.Ala484=
XM_011520400.1:c.1461A>T	XP_011518702.1:p.Ala487=
XM_011520401.1:c.1284A>T	XP_011518703.1:p.Ala428=
XM_011520400.2:c.1461A>T	XP_011518702.1:p.Ala487=
NM_032228.6:c.1452A>T MANE Select	NP_115604.1:p.Ala484=