Canonical Allele Identifier: CA2428551452

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251834C= , CM000685.2:g.49251834C=	GRCh38
NC_000023.10:g.49108295C= , CM000685.1:g.49108295C=	GRCh37
NC_000023.9:g.48995239C=	NCBI36
NG_007392.1:g.17994G= , LRG_62:g.17994G=
NG_021311.2:g.21370C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.940-69G=	ENSP00000365372.2:n.940-69G=
ENST00000376207.10:c.1045-69G= MANE Select	ENSP00000365380.4:n.1045-69G=
ENST00000455775.7:c.1114-69G=	ENSP00000396415.3:n.1114-69G=
ENST00000518685.6:c.964-69G=	ENSP00000428952.2:n.964-69G=
ENST00000557224.6:c.940-69G=	ENSP00000451208.1:n.940-69G=
ENST00000651307.1:c.968-69G=	ENSP00000498454.1:n.968-69G=
ENST00000376197.1:c.895-69G=	ENSP00000365369.1:n.895-69G=
ENST00000376199.6:c.940-69G=	ENSP00000365372.2:n.940-69G=
ENST00000376207.8:c.1045-69G=	ENSP00000365380.4:n.1045-69G=
ENST00000455775.6:c.1114-69G=	ENSP00000396415.3:n.1114-69G=
ENST00000518685.5:c.940-69G=	ENSP00000428952.1:n.940-69G=
ENST00000557224.5:c.940-69G=	ENSP00000451208.1:n.940-69G=
NM_001114377.1:c.940-69G=	NP_001107849.1:n.940-69G=
NM_014009.3:c.1045-69G= , LRG_62t1:c.1045-69G=	NP_054728.2:n.1045-69G=
XM_006724533.2:c.1114-69G=	XP_006724596.2:n.1114-69G=
XM_011543915.1:c.1264-69G=	XP_011542217.1:n.1264-69G=
XM_011543916.1:c.1264-69G=	XP_011542218.1:n.1264-69G=
XM_011543917.1:c.1063-69G=	XP_011542219.1:n.1063-69G=
XM_011543918.1:c.1300-69G=	XP_011542220.1:n.1300-69G=
XM_011543919.1:c.1264-69G=	XP_011542221.1:n.1264-69G=
XM_017029567.1:c.991-69G=	XP_016885056.1:n.991-69G=
NM_001114377.2:c.940-69G=	NP_001107849.1:n.940-69G=
NM_014009.4:c.1045-69G= MANE Select	NP_054728.2:n.1045-69G=