Canonical Allele Identifier: CA516569892

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108206C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251745C>T , CM000685.2:g.49251745C>T	GRCh38
NC_000023.10:g.49108206C>T , CM000685.1:g.49108206C>T	GRCh37
NC_000023.9:g.48995150C>T	NCBI36
NG_007392.1:g.18083G>A , LRG_62:g.18083G>A
NG_021311.2:g.21281C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.960G>A	ENSP00000365372.2:p.Glu320=
ENST00000376207.10:c.1065G>A MANE Select	ENSP00000365380.4:p.Glu355=
ENST00000455775.7:c.1134G>A	ENSP00000396415.3:p.Glu378=
ENST00000518685.6:c.984G>A	ENSP00000428952.2:p.Glu328=
ENST00000557224.6:c.960G>A	ENSP00000451208.1:p.Glu320=
ENST00000651307.1:c.988G>A	ENSP00000498454.1:p.Glu330Lys
ENST00000376197.1:c.915G>A	ENSP00000365369.1:p.Glu305=
ENST00000376199.6:c.960G>A	ENSP00000365372.2:p.Glu320=
ENST00000376207.8:c.1065G>A	ENSP00000365380.4:p.Glu355=
ENST00000455775.6:c.1134G>A	ENSP00000396415.3:p.Glu378=
ENST00000518685.5:c.960G>A	ENSP00000428952.1:p.Glu320=
ENST00000557224.5:c.960G>A	ENSP00000451208.1:p.Glu320=
NM_001114377.1:c.960G>A	NP_001107849.1:p.Glu320=
NM_014009.3:c.1065G>A , LRG_62t1:c.1065G>A	NP_054728.2:p.Glu355=
XM_006724533.2:c.1134G>A	XP_006724596.2:p.Glu378=
XM_011543915.1:c.1284G>A	XP_011542217.1:p.Glu428=
XM_011543916.1:c.1284G>A	XP_011542218.1:p.Glu428=
XM_011543917.1:c.1083G>A	XP_011542219.1:p.Glu361=
XM_011543918.1:c.1320G>A	XP_011542220.1:p.Glu440=
XM_011543919.1:c.1284G>A	XP_011542221.1:p.Glu428=
XM_017029567.1:c.1011G>A	XP_016885056.1:p.Glu337=
NM_001114377.2:c.960G>A	NP_001107849.1:p.Glu320=
NM_014009.4:c.1065G>A MANE Select	NP_054728.2:p.Glu355=