Canonical Allele Identifier: CA412950334

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49109645T>A (hg19) ; chrX:g.49253184T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49253184T>A , CM000685.2:g.49253184T>A	GRCh38
NC_000023.10:g.49109645T>A , CM000685.1:g.49109645T>A	GRCh37
NC_000023.9:g.48996589T>A	NCBI36
NG_007392.1:g.16644A>T , LRG_62:g.16644A>T
NG_021311.2:g.22720T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.881A>T	ENSP00000365372.2:p.Asp294Val
ENST00000376207.10:c.986A>T MANE Select	ENSP00000365380.4:p.Asp329Val
ENST00000455775.7:c.1055A>T	ENSP00000396415.3:p.Asp352Val
ENST00000518685.6:c.905A>T	ENSP00000428952.2:p.Asp302Val
ENST00000557224.6:c.881A>T	ENSP00000451208.1:p.Asp294Val
ENST00000651307.1:c.967+733A>T	ENSP00000498454.1:n.967+733A>T
ENST00000376197.1:c.836A>T	ENSP00000365369.1:p.Asp279Val
ENST00000376199.6:c.881A>T	ENSP00000365372.2:p.Asp294Val
ENST00000376207.8:c.986A>T	ENSP00000365380.4:p.Asp329Val
ENST00000455775.6:c.1055A>T	ENSP00000396415.3:p.Asp352Val
ENST00000518685.5:c.881A>T	ENSP00000428952.1:p.Asp294Val
ENST00000557224.5:c.881A>T	ENSP00000451208.1:p.Asp294Val
NM_001114377.1:c.881A>T	NP_001107849.1:p.Asp294Val
NM_014009.3:c.986A>T , LRG_62t1:c.986A>T	NP_054728.2:p.Asp329Val
XM_006724533.2:c.1055A>T	XP_006724596.2:p.Asp352Val
XM_011543915.1:c.1205A>T	XP_011542217.1:p.Asp402Val
XM_011543916.1:c.1205A>T	XP_011542218.1:p.Asp402Val
XM_011543917.1:c.1004A>T	XP_011542219.1:p.Asp335Val
XM_011543918.1:c.1241A>T	XP_011542220.1:p.Asp414Val
XM_011543919.1:c.1205A>T	XP_011542221.1:p.Asp402Val
XM_017029567.1:c.932A>T	XP_016885056.1:p.Asp311Val
NM_001114377.2:c.881A>T	NP_001107849.1:p.Asp294Val
NM_014009.4:c.986A>T MANE Select	NP_054728.2:p.Asp329Val