Canonical Allele Identifier: CA2428552714

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255737A= , CM000685.2:g.49255737A=	GRCh38
NC_000023.10:g.49112198A= , CM000685.1:g.49112198A=	GRCh37
NC_000023.9:g.48999142A=	NCBI36
NG_007392.1:g.14091T= , LRG_62:g.14091T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.608T=	ENSP00000365372.2:p.Met203=
ENST00000376207.10:c.713T= MANE Select	ENSP00000365380.4:p.Met238=
ENST00000455775.7:c.782T=	ENSP00000396415.3:p.Met261=
ENST00000518685.6:c.713T=	ENSP00000428952.2:p.Met238=
ENST00000557224.6:c.608T=	ENSP00000451208.1:p.Met203=
ENST00000651307.1:c.713T=	ENSP00000498454.1:p.Met238=
ENST00000376197.1:c.563T=	ENSP00000365369.1:p.Met188=
ENST00000376199.6:c.608T=	ENSP00000365372.2:p.Met203=
ENST00000376207.8:c.713T=	ENSP00000365380.4:p.Met238=
ENST00000455775.6:c.782T=	ENSP00000396415.3:p.Met261=
ENST00000518685.5:c.608T=	ENSP00000428952.1:p.Met203=
ENST00000557224.5:c.608T=	ENSP00000451208.1:p.Met203=
NM_001114377.1:c.608T=	NP_001107849.1:p.Met203=
NM_014009.3:c.713T= , LRG_62t1:c.713T=	NP_054728.2:p.Met238=
XM_006724533.2:c.782T=	XP_006724596.2:p.Met261=
XM_011543915.1:c.932T=	XP_011542217.1:p.Met311=
XM_011543916.1:c.932T=	XP_011542218.1:p.Met311=
XM_011543917.1:c.731T=	XP_011542219.1:p.Met244=
XM_011543918.1:c.968T=	XP_011542220.1:p.Met323=
XM_011543919.1:c.932T=	XP_011542221.1:p.Met311=
XM_017029567.1:c.659T=	XP_016885056.1:p.Met220=
NM_001114377.2:c.608T=	NP_001107849.1:p.Met203=
NM_014009.4:c.713T= MANE Select	NP_054728.2:p.Met238=