Canonical Allele Identifier: CA2428551399

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251698A= , CM000685.2:g.49251698A=	GRCh38
NC_000023.10:g.49108159A= , CM000685.1:g.49108159A=	GRCh37
NC_000023.9:g.48995103A=	NCBI36
NG_007392.1:g.18130T= , LRG_62:g.18130T=
NG_021311.2:g.21234A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.1007T=	ENSP00000365372.2:p.Phe336=
ENST00000376207.10:c.1112T= MANE Select	ENSP00000365380.4:p.Phe371=
ENST00000455775.7:c.1181T=	ENSP00000396415.3:p.Phe394=
ENST00000518685.6:c.1031T=	ENSP00000428952.2:p.Phe344=
ENST00000557224.6:c.1007T=	ENSP00000451208.1:p.Phe336=
ENST00000651307.1:c.*27T=	ENSP00000498454.1:n.*27T=
ENST00000376197.1:c.962T=	ENSP00000365369.1:p.Phe321=
ENST00000376199.6:c.1007T=	ENSP00000365372.2:p.Phe336=
ENST00000376207.8:c.1112T=	ENSP00000365380.4:p.Phe371=
ENST00000455775.6:c.1181T=	ENSP00000396415.3:p.Phe394=
ENST00000518685.5:c.1007T=	ENSP00000428952.1:p.Phe336=
ENST00000557224.5:c.1007T=	ENSP00000451208.1:p.Phe336=
NM_001114377.1:c.1007T=	NP_001107849.1:p.Phe336=
NM_014009.3:c.1112T= , LRG_62t1:c.1112T=	NP_054728.2:p.Phe371=
XM_006724533.2:c.1181T=	XP_006724596.2:p.Phe394=
XM_011543915.1:c.1331T=	XP_011542217.1:p.Phe444=
XM_011543916.1:c.1331T=	XP_011542218.1:p.Phe444=
XM_011543917.1:c.1130T=	XP_011542219.1:p.Phe377=
XM_011543918.1:c.1367T=	XP_011542220.1:p.Phe456=
XM_011543919.1:c.1331T=	XP_011542221.1:p.Phe444=
XM_017029567.1:c.1058T=	XP_016885056.1:p.Phe353=
NM_001114377.2:c.1007T=	NP_001107849.1:p.Phe336=
NM_014009.4:c.1112T= MANE Select	NP_054728.2:p.Phe371=