Canonical Allele Identifier: CA2428551774

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49253155G= , CM000685.2:g.49253155G=	GRCh38
NC_000023.10:g.49109616G= , CM000685.1:g.49109616G=	GRCh37
NC_000023.9:g.48996560G=	NCBI36
NG_007392.1:g.16673C= , LRG_62:g.16673C=
NG_021311.2:g.22691G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.910C=	ENSP00000365372.2:p.Pro304=
ENST00000376207.10:c.1015C= MANE Select	ENSP00000365380.4:p.Pro339=
ENST00000455775.7:c.1084C=	ENSP00000396415.3:p.Pro362=
ENST00000518685.6:c.934C=	ENSP00000428952.2:p.Pro312=
ENST00000557224.6:c.910C=	ENSP00000451208.1:p.Pro304=
ENST00000651307.1:c.967+762C=	ENSP00000498454.1:n.967+762C=
ENST00000376197.1:c.865C=	ENSP00000365369.1:p.Pro289=
ENST00000376199.6:c.910C=	ENSP00000365372.2:p.Pro304=
ENST00000376207.8:c.1015C=	ENSP00000365380.4:p.Pro339=
ENST00000455775.6:c.1084C=	ENSP00000396415.3:p.Pro362=
ENST00000518685.5:c.910C=	ENSP00000428952.1:p.Pro304=
ENST00000557224.5:c.910C=	ENSP00000451208.1:p.Pro304=
NM_001114377.1:c.910C=	NP_001107849.1:p.Pro304=
NM_014009.3:c.1015C= , LRG_62t1:c.1015C=	NP_054728.2:p.Pro339=
XM_006724533.2:c.1084C=	XP_006724596.2:p.Pro362=
XM_011543915.1:c.1234C=	XP_011542217.1:p.Pro412=
XM_011543916.1:c.1234C=	XP_011542218.1:p.Pro412=
XM_011543917.1:c.1033C=	XP_011542219.1:p.Pro345=
XM_011543918.1:c.1270C=	XP_011542220.1:p.Pro424=
XM_011543919.1:c.1234C=	XP_011542221.1:p.Pro412=
XM_017029567.1:c.961C=	XP_016885056.1:p.Pro321=
NM_001114377.2:c.910C=	NP_001107849.1:p.Pro304=
NM_014009.4:c.1015C= MANE Select	NP_054728.2:p.Pro339=