Canonical Allele Identifier: CA516569873

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108170G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251709G>A , CM000685.2:g.49251709G>A	GRCh38
NC_000023.10:g.49108170G>A , CM000685.1:g.49108170G>A	GRCh37
NC_000023.9:g.48995114G>A	NCBI36
NG_007392.1:g.18119C>T , LRG_62:g.18119C>T
NG_021311.2:g.21245G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.996C>T	ENSP00000365372.2:p.Phe332=
ENST00000376207.10:c.1101C>T MANE Select	ENSP00000365380.4:p.Phe367=
ENST00000455775.7:c.1170C>T	ENSP00000396415.3:p.Phe390=
ENST00000518685.6:c.1020C>T	ENSP00000428952.2:p.Phe340=
ENST00000557224.6:c.996C>T	ENSP00000451208.1:p.Phe332=
ENST00000651307.1:c.*16C>T	ENSP00000498454.1:n.*16C>T
ENST00000376197.1:c.951C>T	ENSP00000365369.1:p.Phe317=
ENST00000376199.6:c.996C>T	ENSP00000365372.2:p.Phe332=
ENST00000376207.8:c.1101C>T	ENSP00000365380.4:p.Phe367=
ENST00000455775.6:c.1170C>T	ENSP00000396415.3:p.Phe390=
ENST00000518685.5:c.996C>T	ENSP00000428952.1:p.Phe332=
ENST00000557224.5:c.996C>T	ENSP00000451208.1:p.Phe332=
NM_001114377.1:c.996C>T	NP_001107849.1:p.Phe332=
NM_014009.3:c.1101C>T , LRG_62t1:c.1101C>T	NP_054728.2:p.Phe367=
XM_006724533.2:c.1170C>T	XP_006724596.2:p.Phe390=
XM_011543915.1:c.1320C>T	XP_011542217.1:p.Phe440=
XM_011543916.1:c.1320C>T	XP_011542218.1:p.Phe440=
XM_011543917.1:c.1119C>T	XP_011542219.1:p.Phe373=
XM_011543918.1:c.1356C>T	XP_011542220.1:p.Phe452=
XM_011543919.1:c.1320C>T	XP_011542221.1:p.Phe440=
XM_017029567.1:c.1047C>T	XP_016885056.1:p.Phe349=
NM_001114377.2:c.996C>T	NP_001107849.1:p.Phe332=
NM_014009.4:c.1101C>T MANE Select	NP_054728.2:p.Phe367=