Canonical Allele Identifier: CA2428551330

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251441G= , CM000685.2:g.49251441G=	GRCh38
NC_000023.10:g.49107902G= , CM000685.1:g.49107902G=	GRCh37
NC_000023.9:g.48994846G=	NCBI36
NG_007392.1:g.18387C= , LRG_62:g.18387C=
NG_021311.2:g.20977G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.1084C=	ENSP00000365372.2:p.Arg362=
ENST00000376207.10:c.1189C= MANE Select	ENSP00000365380.4:p.Arg397=
ENST00000455775.7:c.1258C=	ENSP00000396415.3:p.Arg420=
ENST00000518685.6:c.1108C=	ENSP00000428952.2:p.Arg370=
ENST00000557224.6:c.1264C=	ENSP00000451208.1:p.Arg422=
ENST00000651307.1:c.*104C=	ENSP00000498454.1:n.*104C=
ENST00000376197.1:c.1219C=	ENSP00000365369.1:p.Arg407=
ENST00000376199.6:c.1084C=	ENSP00000365372.2:p.Arg362=
ENST00000376207.8:c.1189C=	ENSP00000365380.4:p.Arg397=
ENST00000455775.6:c.1258C=	ENSP00000396415.3:p.Arg420=
ENST00000518685.5:c.1084C=	ENSP00000428952.1:p.Arg362=
ENST00000557224.5:c.1264C=	ENSP00000451208.1:p.Arg422=
NM_001114377.1:c.1084C=	NP_001107849.1:p.Arg362=
NM_014009.3:c.1189C= , LRG_62t1:c.1189C=	NP_054728.2:p.Arg397=
XM_006724533.2:c.1258C=	XP_006724596.2:p.Arg420=
XM_011543915.1:c.1588C=	XP_011542217.1:p.Arg530=
XM_011543916.1:c.1588C=	XP_011542218.1:p.Arg530=
XM_011543917.1:c.1207C=	XP_011542219.1:p.Arg403=
XM_011543918.1:c.1444C=	XP_011542220.1:p.Arg482=
XM_011543919.1:c.1408C=	XP_011542221.1:p.Arg470=
XM_017029567.1:c.1315C=	XP_016885056.1:p.Arg439=
NM_001114377.2:c.1084C=	NP_001107849.1:p.Arg362=
NM_014009.4:c.1189C= MANE Select	NP_054728.2:p.Arg397=