Canonical Allele Identifier: CA2428552641

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255484C= , CM000685.2:g.49255484C=	GRCh38
NC_000023.10:g.49111945C= , CM000685.1:g.49111945C=	GRCh37
NC_000023.9:g.48998889C=	NCBI36
NG_007392.1:g.14344G= , LRG_62:g.14344G=
NG_021311.2:g.25020C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.656G=	ENSP00000365372.2:p.Ser219=
ENST00000376207.10:c.761G= MANE Select	ENSP00000365380.4:p.Ser254=
ENST00000455775.7:c.830G=	ENSP00000396415.3:p.Ser277=
ENST00000518685.6:c.735+231G=	ENSP00000428952.2:n.735+231G=
ENST00000557224.6:c.656G=	ENSP00000451208.1:p.Ser219=
ENST00000651307.1:c.761G=	ENSP00000498454.1:p.Ser254=
ENST00000376197.1:c.611G=	ENSP00000365369.1:p.Ser204=
ENST00000376199.6:c.656G=	ENSP00000365372.2:p.Ser219=
ENST00000376207.8:c.761G=	ENSP00000365380.4:p.Ser254=
ENST00000455775.6:c.830G=	ENSP00000396415.3:p.Ser277=
ENST00000518685.5:c.656G=	ENSP00000428952.1:p.Ser219=
ENST00000557224.5:c.656G=	ENSP00000451208.1:p.Ser219=
NM_001114377.1:c.656G=	NP_001107849.1:p.Ser219=
NM_014009.3:c.761G= , LRG_62t1:c.761G=	NP_054728.2:p.Ser254=
XM_006724533.2:c.830G=	XP_006724596.2:p.Ser277=
XM_011543915.1:c.980G=	XP_011542217.1:p.Ser327=
XM_011543916.1:c.980G=	XP_011542218.1:p.Ser327=
XM_011543917.1:c.779G=	XP_011542219.1:p.Ser260=
XM_011543918.1:c.1016G=	XP_011542220.1:p.Ser339=
XM_011543919.1:c.980G=	XP_011542221.1:p.Ser327=
XM_017029567.1:c.707G=	XP_016885056.1:p.Ser236=
NM_001114377.2:c.656G=	NP_001107849.1:p.Ser219=
NM_014009.4:c.761G= MANE Select	NP_054728.2:p.Ser254=