Canonical Allele Identifier: CA2428551810

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49253175T= , CM000685.2:g.49253175T=	GRCh38
NC_000023.10:g.49109636T= , CM000685.1:g.49109636T=	GRCh37
NC_000023.9:g.48996580T=	NCBI36
NG_007392.1:g.16653A= , LRG_62:g.16653A=
NG_021311.2:g.22711T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.890A=	ENSP00000365372.2:p.Lys297=
ENST00000376207.10:c.995A= MANE Select	ENSP00000365380.4:p.Lys332=
ENST00000455775.7:c.1064A=	ENSP00000396415.3:p.Lys355=
ENST00000518685.6:c.914A=	ENSP00000428952.2:p.Lys305=
ENST00000557224.6:c.890A=	ENSP00000451208.1:p.Lys297=
ENST00000651307.1:c.967+742A=	ENSP00000498454.1:n.967+742A=
ENST00000376197.1:c.845A=	ENSP00000365369.1:p.Lys282=
ENST00000376199.6:c.890A=	ENSP00000365372.2:p.Lys297=
ENST00000376207.8:c.995A=	ENSP00000365380.4:p.Lys332=
ENST00000455775.6:c.1064A=	ENSP00000396415.3:p.Lys355=
ENST00000518685.5:c.890A=	ENSP00000428952.1:p.Lys297=
ENST00000557224.5:c.890A=	ENSP00000451208.1:p.Lys297=
NM_001114377.1:c.890A=	NP_001107849.1:p.Lys297=
NM_014009.3:c.995A= , LRG_62t1:c.995A=	NP_054728.2:p.Lys332=
XM_006724533.2:c.1064A=	XP_006724596.2:p.Lys355=
XM_011543915.1:c.1214A=	XP_011542217.1:p.Lys405=
XM_011543916.1:c.1214A=	XP_011542218.1:p.Lys405=
XM_011543917.1:c.1013A=	XP_011542219.1:p.Lys338=
XM_011543918.1:c.1250A=	XP_011542220.1:p.Lys417=
XM_011543919.1:c.1214A=	XP_011542221.1:p.Lys405=
XM_017029567.1:c.941A=	XP_016885056.1:p.Lys314=
NM_001114377.2:c.890A=	NP_001107849.1:p.Lys297=
NM_014009.4:c.995A= MANE Select	NP_054728.2:p.Lys332=