Canonical Allele Identifier: CA412949053

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108226C>T (hg19) ; chrX:g.49251765C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251765C>T , CM000685.2:g.49251765C>T	GRCh38
NC_000023.10:g.49108226C>T , CM000685.1:g.49108226C>T	GRCh37
NC_000023.9:g.48995170C>T	NCBI36
NG_007392.1:g.18063G>A , LRG_62:g.18063G>A
NG_021311.2:g.21301C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.940G>A	ENSP00000365372.2:p.Ala314Thr
ENST00000376207.10:c.1045G>A MANE Select	ENSP00000365380.4:p.Ala349Thr
ENST00000455775.7:c.1114G>A	ENSP00000396415.3:p.Ala372Thr
ENST00000518685.6:c.964G>A	ENSP00000428952.2:p.Ala322Thr
ENST00000557224.6:c.940G>A	ENSP00000451208.1:p.Ala314Thr
ENST00000651307.1:c.968G>A	ENSP00000498454.1:p.Gly323Asp
ENST00000376197.1:c.895G>A	ENSP00000365369.1:p.Ala299Thr
ENST00000376199.6:c.940G>A	ENSP00000365372.2:p.Ala314Thr
ENST00000376207.8:c.1045G>A	ENSP00000365380.4:p.Ala349Thr
ENST00000455775.6:c.1114G>A	ENSP00000396415.3:p.Ala372Thr
ENST00000518685.5:c.940G>A	ENSP00000428952.1:p.Ala314Thr
ENST00000557224.5:c.940G>A	ENSP00000451208.1:p.Ala314Thr
NM_001114377.1:c.940G>A	NP_001107849.1:p.Ala314Thr
NM_014009.3:c.1045G>A , LRG_62t1:c.1045G>A	NP_054728.2:p.Ala349Thr
XM_006724533.2:c.1114G>A	XP_006724596.2:p.Ala372Thr
XM_011543915.1:c.1264G>A	XP_011542217.1:p.Ala422Thr
XM_011543916.1:c.1264G>A	XP_011542218.1:p.Ala422Thr
XM_011543917.1:c.1063G>A	XP_011542219.1:p.Ala355Thr
XM_011543918.1:c.1300G>A	XP_011542220.1:p.Ala434Thr
XM_011543919.1:c.1264G>A	XP_011542221.1:p.Ala422Thr
XM_017029567.1:c.991G>A	XP_016885056.1:p.Ala331Thr
NM_001114377.2:c.940G>A	NP_001107849.1:p.Ala314Thr
NM_014009.4:c.1045G>A MANE Select	NP_054728.2:p.Ala349Thr