Canonical Allele Identifier: CA2428551404

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251711A= , CM000685.2:g.49251711A=	GRCh38
NC_000023.10:g.49108172A= , CM000685.1:g.49108172A=	GRCh37
NC_000023.9:g.48995116A=	NCBI36
NG_007392.1:g.18117T= , LRG_62:g.18117T=
NG_021311.2:g.21247A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.994T=	ENSP00000365372.2:p.Phe332=
ENST00000376207.10:c.1099T= MANE Select	ENSP00000365380.4:p.Phe367=
ENST00000455775.7:c.1168T=	ENSP00000396415.3:p.Phe390=
ENST00000518685.6:c.1018T=	ENSP00000428952.2:p.Phe340=
ENST00000557224.6:c.994T=	ENSP00000451208.1:p.Phe332=
ENST00000651307.1:c.*14T=	ENSP00000498454.1:n.*14T=
ENST00000376197.1:c.949T=	ENSP00000365369.1:p.Phe317=
ENST00000376199.6:c.994T=	ENSP00000365372.2:p.Phe332=
ENST00000376207.8:c.1099T=	ENSP00000365380.4:p.Phe367=
ENST00000455775.6:c.1168T=	ENSP00000396415.3:p.Phe390=
ENST00000518685.5:c.994T=	ENSP00000428952.1:p.Phe332=
ENST00000557224.5:c.994T=	ENSP00000451208.1:p.Phe332=
NM_001114377.1:c.994T=	NP_001107849.1:p.Phe332=
NM_014009.3:c.1099T= , LRG_62t1:c.1099T=	NP_054728.2:p.Phe367=
XM_006724533.2:c.1168T=	XP_006724596.2:p.Phe390=
XM_011543915.1:c.1318T=	XP_011542217.1:p.Phe440=
XM_011543916.1:c.1318T=	XP_011542218.1:p.Phe440=
XM_011543917.1:c.1117T=	XP_011542219.1:p.Phe373=
XM_011543918.1:c.1354T=	XP_011542220.1:p.Phe452=
XM_011543919.1:c.1318T=	XP_011542221.1:p.Phe440=
XM_017029567.1:c.1045T=	XP_016885056.1:p.Phe349=
NM_001114377.2:c.994T=	NP_001107849.1:p.Phe332=
NM_014009.4:c.1099T= MANE Select	NP_054728.2:p.Phe367=