Canonical Allele Identifier: CA2428551334

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251480C= , CM000685.2:g.49251480C=	GRCh38
NC_000023.10:g.49107941C= , CM000685.1:g.49107941C=	GRCh37
NC_000023.9:g.48994885C=	NCBI36
NG_007392.1:g.18348G= , LRG_62:g.18348G=
NG_021311.2:g.21016C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.1045G=	ENSP00000365372.2:p.Ala349=
ENST00000376207.10:c.1150G= MANE Select	ENSP00000365380.4:p.Ala384=
ENST00000455775.7:c.1219G=	ENSP00000396415.3:p.Ala407=
ENST00000518685.6:c.1069G=	ENSP00000428952.2:p.Ala357=
ENST00000557224.6:c.1225G=	ENSP00000451208.1:p.Ala409=
ENST00000651307.1:c.*65G=	ENSP00000498454.1:n.*65G=
ENST00000376197.1:c.1180G=	ENSP00000365369.1:p.Ala394=
ENST00000376199.6:c.1045G=	ENSP00000365372.2:p.Ala349=
ENST00000376207.8:c.1150G=	ENSP00000365380.4:p.Ala384=
ENST00000455775.6:c.1219G=	ENSP00000396415.3:p.Ala407=
ENST00000518685.5:c.1045G=	ENSP00000428952.1:p.Ala349=
ENST00000557224.5:c.1225G=	ENSP00000451208.1:p.Ala409=
NM_001114377.1:c.1045G=	NP_001107849.1:p.Ala349=
NM_014009.3:c.1150G= , LRG_62t1:c.1150G=	NP_054728.2:p.Ala384=
XM_006724533.2:c.1219G=	XP_006724596.2:p.Ala407=
XM_011543915.1:c.1549G=	XP_011542217.1:p.Ala517=
XM_011543916.1:c.1549G=	XP_011542218.1:p.Ala517=
XM_011543917.1:c.1168G=	XP_011542219.1:p.Ala390=
XM_011543918.1:c.1405G=	XP_011542220.1:p.Ala469=
XM_011543919.1:c.1369G=	XP_011542221.1:p.Ala457=
XM_017029567.1:c.1276G=	XP_016885056.1:p.Ala426=
NM_001114377.2:c.1045G=	NP_001107849.1:p.Ala349=
NM_014009.4:c.1150G= MANE Select	NP_054728.2:p.Ala384=