Canonical Allele Identifier: CA1953439072

Gene: FAR1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13728582G= , CM000673.2:g.13728582G=	GRCh38
NC_000011.9:g.13750129G= , CM000673.1:g.13750129G=	GRCh37
NC_000011.8:g.13706705G=	NCBI36
NG_041826.1:g.64924G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703358.1:c.*211-30G=	ENSP00000515269.1:n.*211-30G=
ENST00000354817.8:c.1386-30G= MANE Select	ENSP00000346874.3:n.1386-30G=
ENST00000354817.7:c.1386-30G=	ENSP00000346874.3:n.1386-30G=
ENST00000532502.1:c.258-30G=	ENSP00000434624.1:n.258-30G=
NM_032228.5:c.1386-30G=	NP_115604.1:n.1386-30G=
XM_011520400.1:c.1395-30G=	XP_011518702.1:n.1395-30G=
XM_011520401.1:c.1218-30G=	XP_011518703.1:n.1218-30G=
XM_011520400.2:c.1395-30G=	XP_011518702.1:n.1395-30G=
NM_032228.6:c.1386-30G= MANE Select	NP_115604.1:n.1386-30G=