Canonical Allele Identifier: CA412949013

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108216T>A (hg19) ; chrX:g.49251755T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251755T>A , CM000685.2:g.49251755T>A	GRCh38
NC_000023.10:g.49108216T>A , CM000685.1:g.49108216T>A	GRCh37
NC_000023.9:g.48995160T>A	NCBI36
NG_007392.1:g.18073A>T , LRG_62:g.18073A>T
NG_021311.2:g.21291T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.950A>T	ENSP00000365372.2:p.Glu317Val
ENST00000376207.10:c.1055A>T MANE Select	ENSP00000365380.4:p.Glu352Val
ENST00000455775.7:c.1124A>T	ENSP00000396415.3:p.Glu375Val
ENST00000518685.6:c.974A>T	ENSP00000428952.2:p.Glu325Val
ENST00000557224.6:c.950A>T	ENSP00000451208.1:p.Glu317Val
ENST00000651307.1:c.978A>T	ENSP00000498454.1:p.Gly326=
ENST00000376197.1:c.905A>T	ENSP00000365369.1:p.Glu302Val
ENST00000376199.6:c.950A>T	ENSP00000365372.2:p.Glu317Val
ENST00000376207.8:c.1055A>T	ENSP00000365380.4:p.Glu352Val
ENST00000455775.6:c.1124A>T	ENSP00000396415.3:p.Glu375Val
ENST00000518685.5:c.950A>T	ENSP00000428952.1:p.Glu317Val
ENST00000557224.5:c.950A>T	ENSP00000451208.1:p.Glu317Val
NM_001114377.1:c.950A>T	NP_001107849.1:p.Glu317Val
NM_014009.3:c.1055A>T , LRG_62t1:c.1055A>T	NP_054728.2:p.Glu352Val
XM_006724533.2:c.1124A>T	XP_006724596.2:p.Glu375Val
XM_011543915.1:c.1274A>T	XP_011542217.1:p.Glu425Val
XM_011543916.1:c.1274A>T	XP_011542218.1:p.Glu425Val
XM_011543917.1:c.1073A>T	XP_011542219.1:p.Glu358Val
XM_011543918.1:c.1310A>T	XP_011542220.1:p.Glu437Val
XM_011543919.1:c.1274A>T	XP_011542221.1:p.Glu425Val
XM_017029567.1:c.1001A>T	XP_016885056.1:p.Glu334Val
NM_001114377.2:c.950A>T	NP_001107849.1:p.Glu317Val
NM_014009.4:c.1055A>T MANE Select	NP_054728.2:p.Glu352Val