Canonical Allele Identifier: CA2428551373

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251615C= , CM000685.2:g.49251615C=	GRCh38
NC_000023.10:g.49108076C= , CM000685.1:g.49108076C=	GRCh37
NC_000023.9:g.48995020C=	NCBI36
NG_007392.1:g.18213G= , LRG_62:g.18213G=
NG_021311.2:g.21151C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.1041+49G=	ENSP00000365372.2:n.1041+49G=
ENST00000376207.10:c.1146+49G= MANE Select	ENSP00000365380.4:n.1146+49G=
ENST00000455775.7:c.1215+49G=	ENSP00000396415.3:n.1215+49G=
ENST00000518685.6:c.1065+49G=	ENSP00000428952.2:n.1065+49G=
ENST00000557224.6:c.1090G=	ENSP00000451208.1:p.Ala364=
ENST00000651307.1:c.*61+49G=	ENSP00000498454.1:n.*61+49G=
ENST00000376197.1:c.1045G=	ENSP00000365369.1:p.Ala349=
ENST00000376199.6:c.1041+49G=	ENSP00000365372.2:n.1041+49G=
ENST00000376207.8:c.1146+49G=	ENSP00000365380.4:n.1146+49G=
ENST00000455775.6:c.1215+49G=	ENSP00000396415.3:n.1215+49G=
ENST00000518685.5:c.1041+49G=	ENSP00000428952.1:n.1041+49G=
ENST00000557224.5:c.1090G=	ENSP00000451208.1:p.Ala364=
NM_001114377.1:c.1041+49G=	NP_001107849.1:n.1041+49G=
NM_014009.3:c.1146+49G= , LRG_62t1:c.1146+49G=	NP_054728.2:n.1146+49G=
XM_006724533.2:c.1215+49G=	XP_006724596.2:n.1215+49G=
XM_011543915.1:c.1414G=	XP_011542217.1:p.Ala472=
XM_011543916.1:c.1414G=	XP_011542218.1:p.Ala472=
XM_011543917.1:c.1164+49G=	XP_011542219.1:n.1164+49G=
XM_011543918.1:c.1401+49G=	XP_011542220.1:n.1401+49G=
XM_011543919.1:c.1365+49G=	XP_011542221.1:n.1365+49G=
XM_017029567.1:c.1141G=	XP_016885056.1:p.Ala381=
NM_001114377.2:c.1041+49G=	NP_001107849.1:n.1041+49G=
NM_014009.4:c.1146+49G= MANE Select	NP_054728.2:n.1146+49G=