Canonical Allele Identifier: CA516397341

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49112194T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255733T>A , CM000685.2:g.49255733T>A	GRCh38
NC_000023.10:g.49112194T>A , CM000685.1:g.49112194T>A	GRCh37
NC_000023.9:g.48999138T>A	NCBI36
NG_007392.1:g.14095A>T , LRG_62:g.14095A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.612A>T	ENSP00000365372.2:p.Val204=
ENST00000376207.10:c.717A>T MANE Select	ENSP00000365380.4:p.Val239=
ENST00000455775.7:c.786A>T	ENSP00000396415.3:p.Val262=
ENST00000518685.6:c.717A>T	ENSP00000428952.2:p.Val239=
ENST00000557224.6:c.612A>T	ENSP00000451208.1:p.Val204=
ENST00000651307.1:c.717A>T	ENSP00000498454.1:p.Val239=
ENST00000376197.1:c.567A>T	ENSP00000365369.1:p.Val189=
ENST00000376199.6:c.612A>T	ENSP00000365372.2:p.Val204=
ENST00000376207.8:c.717A>T	ENSP00000365380.4:p.Val239=
ENST00000455775.6:c.786A>T	ENSP00000396415.3:p.Val262=
ENST00000518685.5:c.612A>T	ENSP00000428952.1:p.Val204=
ENST00000557224.5:c.612A>T	ENSP00000451208.1:p.Val204=
NM_001114377.1:c.612A>T	NP_001107849.1:p.Val204=
NM_014009.3:c.717A>T , LRG_62t1:c.717A>T	NP_054728.2:p.Val239=
XM_006724533.2:c.786A>T	XP_006724596.2:p.Val262=
XM_011543915.1:c.936A>T	XP_011542217.1:p.Val312=
XM_011543916.1:c.936A>T	XP_011542218.1:p.Val312=
XM_011543917.1:c.735A>T	XP_011542219.1:p.Val245=
XM_011543918.1:c.972A>T	XP_011542220.1:p.Val324=
XM_011543919.1:c.936A>T	XP_011542221.1:p.Val312=
XM_017029567.1:c.663A>T	XP_016885056.1:p.Val221=
NM_001114377.2:c.612A>T	NP_001107849.1:p.Val204=
NM_014009.4:c.717A>T MANE Select	NP_054728.2:p.Val239=