Canonical Allele Identifier: CA2695233611

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251750del , CM000685.2:g.49251750del	GRCh38
NC_000023.10:g.49108211del , CM000685.1:g.49108211del	GRCh37
NC_000023.9:g.48995155del	NCBI36
NG_007392.1:g.18079del , LRG_62:g.18079del
NG_021311.2:g.21286del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.956del	ENSP00000365372.2:p.Pro319GlnfsTer?
ENST00000376207.10:c.1061del MANE Select	ENSP00000365380.4:p.Pro354GlnfsTer?
ENST00000455775.7:c.1130del	ENSP00000396415.3:p.Pro377GlnfsTer?
ENST00000518685.6:c.980del	ENSP00000428952.2:p.Pro327GlnfsTer?
ENST00000557224.6:c.956del	ENSP00000451208.1:p.Pro319GlnfsTer30
ENST00000651307.1:c.984del	ENSP00000498454.1:p.Arg329GlufsTer?
ENST00000376197.1:c.911del	ENSP00000365369.1:p.Pro304GlnfsTer30
ENST00000376199.6:c.956del	ENSP00000365372.2:p.Pro319GlnfsTer?
ENST00000376207.8:c.1061del	ENSP00000365380.4:p.Pro354GlnfsTer?
ENST00000455775.6:c.1130del	ENSP00000396415.3:p.Pro377GlnfsTer?
ENST00000518685.5:c.956del	ENSP00000428952.1:p.Pro319GlnfsTer?
ENST00000557224.5:c.956del	ENSP00000451208.1:p.Pro319GlnfsTer30
NM_001114377.1:c.956del	NP_001107849.1:p.Pro319GlnfsTer?
NM_014009.3:c.1061del , LRG_62t1:c.1061del	NP_054728.2:p.Pro354GlnfsTer?
XM_006724533.2:c.1130del	XP_006724596.2:p.Pro377GlnfsTer?
XM_011543915.1:c.1280del	XP_011542217.1:p.Pro427GlnfsTer30
XM_011543916.1:c.1280del	XP_011542218.1:p.Pro427GlnfsTer30
XM_011543917.1:c.1079del	XP_011542219.1:p.Pro360GlnfsTer?
XM_011543918.1:c.1316del	XP_011542220.1:p.Pro439GlnfsTer?
XM_011543919.1:c.1280del	XP_011542221.1:p.Pro427GlnfsTer?
XM_017029567.1:c.1007del	XP_016885056.1:p.Pro336GlnfsTer30
NM_001114377.2:c.956del	NP_001107849.1:p.Pro319GlnfsTer?
NM_014009.4:c.1061del MANE Select	NP_054728.2:p.Pro354GlnfsTer?