Canonical Allele Identifier: CA2428553619

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49258476C= , CM000685.2:g.49258476C=	GRCh38
NC_000023.10:g.49114933C= , CM000685.1:g.49114933C=	GRCh37
NC_000023.9:g.49001877C=	NCBI36
NG_007392.1:g.11356G= , LRG_62:g.11356G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703450.1:c.30G=	ENSP00000515301.1:p.Ser10=
ENST00000684155.1:c.30G=	ENSP00000507726.1:p.Ser10=
ENST00000376199.7:c.30G=	ENSP00000365372.2:p.Ser10=
ENST00000376207.10:c.30G= MANE Select	ENSP00000365380.4:p.Ser10=
ENST00000455775.7:c.30G=	ENSP00000396415.3:p.Ser10=
ENST00000518685.6:c.30G=	ENSP00000428952.2:p.Ser10=
ENST00000557224.6:c.30G=	ENSP00000451208.1:p.Ser10=
ENST00000650877.1:c.30G=	ENSP00000499100.1:p.Ser10=
ENST00000651307.1:c.30G=	ENSP00000498454.1:p.Ser10=
ENST00000652559.1:c.30G=	ENSP00000498236.1:p.Ser10=
ENST00000376197.1:c.17-32G=	ENSP00000365369.1:n.17-32G=
ENST00000376199.6:c.30G=	ENSP00000365372.2:p.Ser10=
ENST00000376207.8:c.30G=	ENSP00000365380.4:p.Ser10=
ENST00000455775.6:c.30G=	ENSP00000396415.3:p.Ser10=
ENST00000518685.5:c.30G=	ENSP00000428952.1:p.Ser10=
ENST00000557224.5:c.30G=	ENSP00000451208.1:p.Ser10=
NM_001114377.1:c.30G=	NP_001107849.1:p.Ser10=
NM_014009.3:c.30G= , LRG_62t1:c.30G=	NP_054728.2:p.Ser10=
XM_006724533.2:c.30G=	XP_006724596.2:p.Ser10=
XM_011543915.1:c.354G=	XP_011542217.1:p.Ser118=
XM_011543916.1:c.354G=	XP_011542218.1:p.Ser118=
XM_011543917.1:c.30G=	XP_011542219.1:p.Ser10=
XM_011543918.1:c.354G=	XP_011542220.1:p.Ser118=
XM_011543919.1:c.354G=	XP_011542221.1:p.Ser118=
XM_017029567.1:c.81G=	XP_016885056.1:p.Ser27=
NM_001114377.2:c.30G=	NP_001107849.1:p.Ser10=
NM_014009.4:c.30G= MANE Select	NP_054728.2:p.Ser10=