Canonical Allele Identifier: CA2428551499

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251972G= , CM000685.2:g.49251972G=	GRCh38
NC_000023.10:g.49108433G= , CM000685.1:g.49108433G=	GRCh37
NC_000023.9:g.48995377G=	NCBI36
NG_007392.1:g.17856C= , LRG_62:g.17856C=
NG_021311.2:g.21508G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.940-207C=	ENSP00000365372.2:n.940-207C=
ENST00000376207.10:c.1045-207C= MANE Select	ENSP00000365380.4:n.1045-207C=
ENST00000455775.7:c.1114-207C=	ENSP00000396415.3:n.1114-207C=
ENST00000518685.6:c.964-207C=	ENSP00000428952.2:n.964-207C=
ENST00000557224.6:c.940-207C=	ENSP00000451208.1:n.940-207C=
ENST00000651307.1:c.968-207C=	ENSP00000498454.1:n.968-207C=
ENST00000376197.1:c.895-207C=	ENSP00000365369.1:n.895-207C=
ENST00000376199.6:c.940-207C=	ENSP00000365372.2:n.940-207C=
ENST00000376207.8:c.1045-207C=	ENSP00000365380.4:n.1045-207C=
ENST00000455775.6:c.1114-207C=	ENSP00000396415.3:n.1114-207C=
ENST00000518685.5:c.940-207C=	ENSP00000428952.1:n.940-207C=
ENST00000557224.5:c.940-207C=	ENSP00000451208.1:n.940-207C=
NM_001114377.1:c.940-207C=	NP_001107849.1:n.940-207C=
NM_014009.3:c.1045-207C= , LRG_62t1:c.1045-207C=	NP_054728.2:n.1045-207C=
XM_006724533.2:c.1114-207C=	XP_006724596.2:n.1114-207C=
XM_011543915.1:c.1264-207C=	XP_011542217.1:n.1264-207C=
XM_011543916.1:c.1264-207C=	XP_011542218.1:n.1264-207C=
XM_011543917.1:c.1063-207C=	XP_011542219.1:n.1063-207C=
XM_011543918.1:c.1300-207C=	XP_011542220.1:n.1300-207C=
XM_011543919.1:c.1264-207C=	XP_011542221.1:n.1264-207C=
XM_017029567.1:c.991-207C=	XP_016885056.1:n.991-207C=
NM_001114377.2:c.940-207C=	NP_001107849.1:n.940-207C=
NM_014009.4:c.1045-207C= MANE Select	NP_054728.2:n.1045-207C=