Canonical Allele Identifier: CA1953439105

Gene: FAR1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13728675T= , CM000673.2:g.13728675T=	GRCh38
NC_000011.9:g.13750222T= , CM000673.1:g.13750222T=	GRCh37
NC_000011.8:g.13706798T=	NCBI36
NG_041826.1:g.65017T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703358.1:c.*274T=	ENSP00000515269.1:n.*274T=
ENST00000354817.8:c.1449T= MANE Select	ENSP00000346874.3:p.Ile483=
ENST00000354817.7:c.1449T=	ENSP00000346874.3:p.Ile483=
ENST00000532502.1:c.321T=	ENSP00000434624.1:p.Ile107=
NM_032228.5:c.1449T=	NP_115604.1:p.Ile483=
XM_011520400.1:c.1458T=	XP_011518702.1:p.Ile486=
XM_011520401.1:c.1281T=	XP_011518703.1:p.Ile427=
XM_011520400.2:c.1458T=	XP_011518702.1:p.Ile486=
NM_032228.6:c.1449T= MANE Select	NP_115604.1:p.Ile483=