Canonical Allele Identifier: CA2428551408

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251734G= , CM000685.2:g.49251734G=	GRCh38
NC_000023.10:g.49108195G= , CM000685.1:g.49108195G=	GRCh37
NC_000023.9:g.48995139G=	NCBI36
NG_007392.1:g.18094C= , LRG_62:g.18094C=
NG_021311.2:g.21270G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.971C=	ENSP00000365372.2:p.Thr324=
ENST00000376207.10:c.1076C= MANE Select	ENSP00000365380.4:p.Thr359=
ENST00000455775.7:c.1145C=	ENSP00000396415.3:p.Thr382=
ENST00000518685.6:c.995C=	ENSP00000428952.2:p.Thr332=
ENST00000557224.6:c.971C=	ENSP00000451208.1:p.Thr324=
ENST00000651307.1:c.999C=	ENSP00000498454.1:p.Asp333=
ENST00000376197.1:c.926C=	ENSP00000365369.1:p.Thr309=
ENST00000376199.6:c.971C=	ENSP00000365372.2:p.Thr324=
ENST00000376207.8:c.1076C=	ENSP00000365380.4:p.Thr359=
ENST00000455775.6:c.1145C=	ENSP00000396415.3:p.Thr382=
ENST00000518685.5:c.971C=	ENSP00000428952.1:p.Thr324=
ENST00000557224.5:c.971C=	ENSP00000451208.1:p.Thr324=
NM_001114377.1:c.971C=	NP_001107849.1:p.Thr324=
NM_014009.3:c.1076C= , LRG_62t1:c.1076C=	NP_054728.2:p.Thr359=
XM_006724533.2:c.1145C=	XP_006724596.2:p.Thr382=
XM_011543915.1:c.1295C=	XP_011542217.1:p.Thr432=
XM_011543916.1:c.1295C=	XP_011542218.1:p.Thr432=
XM_011543917.1:c.1094C=	XP_011542219.1:p.Thr365=
XM_011543918.1:c.1331C=	XP_011542220.1:p.Thr444=
XM_011543919.1:c.1295C=	XP_011542221.1:p.Thr432=
XM_017029567.1:c.1022C=	XP_016885056.1:p.Thr341=
NM_001114377.2:c.971C=	NP_001107849.1:p.Thr324=
NM_014009.4:c.1076C= MANE Select	NP_054728.2:p.Thr359=