Canonical Allele Identifier: CA2428552637

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255467G= , CM000685.2:g.49255467G=	GRCh38
NC_000023.10:g.49111928G= , CM000685.1:g.49111928G=	GRCh37
NC_000023.9:g.48998872G=	NCBI36
NG_007392.1:g.14361C= , LRG_62:g.14361C=
NG_021311.2:g.25003G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.673C=	ENSP00000365372.2:p.Leu225=
ENST00000376207.10:c.778C= MANE Select	ENSP00000365380.4:p.Leu260=
ENST00000455775.7:c.847C=	ENSP00000396415.3:p.Leu283=
ENST00000518685.6:c.735+248C=	ENSP00000428952.2:n.735+248C=
ENST00000557224.6:c.673C=	ENSP00000451208.1:p.Leu225=
ENST00000651307.1:c.778C=	ENSP00000498454.1:p.Leu260=
ENST00000376197.1:c.628C=	ENSP00000365369.1:p.Leu210=
ENST00000376199.6:c.673C=	ENSP00000365372.2:p.Leu225=
ENST00000376207.8:c.778C=	ENSP00000365380.4:p.Leu260=
ENST00000455775.6:c.847C=	ENSP00000396415.3:p.Leu283=
ENST00000518685.5:c.673C=	ENSP00000428952.1:p.Leu225=
ENST00000557224.5:c.673C=	ENSP00000451208.1:p.Leu225=
NM_001114377.1:c.673C=	NP_001107849.1:p.Leu225=
NM_014009.3:c.778C= , LRG_62t1:c.778C=	NP_054728.2:p.Leu260=
XM_006724533.2:c.847C=	XP_006724596.2:p.Leu283=
XM_011543915.1:c.997C=	XP_011542217.1:p.Leu333=
XM_011543916.1:c.997C=	XP_011542218.1:p.Leu333=
XM_011543917.1:c.796C=	XP_011542219.1:p.Leu266=
XM_011543918.1:c.1033C=	XP_011542220.1:p.Leu345=
XM_011543919.1:c.997C=	XP_011542221.1:p.Leu333=
XM_017029567.1:c.724C=	XP_016885056.1:p.Leu242=
NM_001114377.2:c.673C=	NP_001107849.1:p.Leu225=
NM_014009.4:c.778C= MANE Select	NP_054728.2:p.Leu260=