Canonical Allele Identifier: CA2428551409

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251737C= , CM000685.2:g.49251737C=	GRCh38
NC_000023.10:g.49108198C= , CM000685.1:g.49108198C=	GRCh37
NC_000023.9:g.48995142C=	NCBI36
NG_007392.1:g.18091G= , LRG_62:g.18091G=
NG_021311.2:g.21273C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.968G=	ENSP00000365372.2:p.Arg323=
ENST00000376207.10:c.1073G= MANE Select	ENSP00000365380.4:p.Arg358=
ENST00000455775.7:c.1142G=	ENSP00000396415.3:p.Arg381=
ENST00000518685.6:c.992G=	ENSP00000428952.2:p.Arg331=
ENST00000557224.6:c.968G=	ENSP00000451208.1:p.Arg323=
ENST00000651307.1:c.996G=	ENSP00000498454.1:p.Ala332=
ENST00000376197.1:c.923G=	ENSP00000365369.1:p.Arg308=
ENST00000376199.6:c.968G=	ENSP00000365372.2:p.Arg323=
ENST00000376207.8:c.1073G=	ENSP00000365380.4:p.Arg358=
ENST00000455775.6:c.1142G=	ENSP00000396415.3:p.Arg381=
ENST00000518685.5:c.968G=	ENSP00000428952.1:p.Arg323=
ENST00000557224.5:c.968G=	ENSP00000451208.1:p.Arg323=
NM_001114377.1:c.968G=	NP_001107849.1:p.Arg323=
NM_014009.3:c.1073G= , LRG_62t1:c.1073G=	NP_054728.2:p.Arg358=
XM_006724533.2:c.1142G=	XP_006724596.2:p.Arg381=
XM_011543915.1:c.1292G=	XP_011542217.1:p.Arg431=
XM_011543916.1:c.1292G=	XP_011542218.1:p.Arg431=
XM_011543917.1:c.1091G=	XP_011542219.1:p.Arg364=
XM_011543918.1:c.1328G=	XP_011542220.1:p.Arg443=
XM_011543919.1:c.1292G=	XP_011542221.1:p.Arg431=
XM_017029567.1:c.1019G=	XP_016885056.1:p.Arg340=
NM_001114377.2:c.968G=	NP_001107849.1:p.Arg323=
NM_014009.4:c.1073G= MANE Select	NP_054728.2:p.Arg358=