Canonical Allele Identifier: CA2428551371

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251608T= , CM000685.2:g.49251608T=	GRCh38
NC_000023.10:g.49108069T= , CM000685.1:g.49108069T=	GRCh37
NC_000023.9:g.48995013T=	NCBI36
NG_007392.1:g.18220A= , LRG_62:g.18220A=
NG_021311.2:g.21144T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.1041+56A=	ENSP00000365372.2:n.1041+56A=
ENST00000376207.10:c.1146+56A= MANE Select	ENSP00000365380.4:n.1146+56A=
ENST00000455775.7:c.1215+56A=	ENSP00000396415.3:n.1215+56A=
ENST00000518685.6:c.1065+56A=	ENSP00000428952.2:n.1065+56A=
ENST00000557224.6:c.1097A=	ENSP00000451208.1:p.Gln366=
ENST00000651307.1:c.*61+56A=	ENSP00000498454.1:n.*61+56A=
ENST00000376197.1:c.1052A=	ENSP00000365369.1:p.Gln351=
ENST00000376199.6:c.1041+56A=	ENSP00000365372.2:n.1041+56A=
ENST00000376207.8:c.1146+56A=	ENSP00000365380.4:n.1146+56A=
ENST00000455775.6:c.1215+56A=	ENSP00000396415.3:n.1215+56A=
ENST00000518685.5:c.1041+56A=	ENSP00000428952.1:n.1041+56A=
ENST00000557224.5:c.1097A=	ENSP00000451208.1:p.Gln366=
NM_001114377.1:c.1041+56A=	NP_001107849.1:n.1041+56A=
NM_014009.3:c.1146+56A= , LRG_62t1:c.1146+56A=	NP_054728.2:n.1146+56A=
XM_006724533.2:c.1215+56A=	XP_006724596.2:n.1215+56A=
XM_011543915.1:c.1421A=	XP_011542217.1:p.Gln474=
XM_011543916.1:c.1421A=	XP_011542218.1:p.Gln474=
XM_011543917.1:c.1164+56A=	XP_011542219.1:n.1164+56A=
XM_011543918.1:c.1401+56A=	XP_011542220.1:n.1401+56A=
XM_011543919.1:c.1365+56A=	XP_011542221.1:n.1365+56A=
XM_017029567.1:c.1148A=	XP_016885056.1:p.Gln383=
NM_001114377.2:c.1041+56A=	NP_001107849.1:n.1041+56A=
NM_014009.4:c.1146+56A= MANE Select	NP_054728.2:n.1146+56A=