Canonical Allele Identifier: CA412950309

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49109640A>T (hg19) ; chrX:g.49253179A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49253179A>T , CM000685.2:g.49253179A>T	GRCh38
NC_000023.10:g.49109640A>T , CM000685.1:g.49109640A>T	GRCh37
NC_000023.9:g.48996584A>T	NCBI36
NG_007392.1:g.16649T>A , LRG_62:g.16649T>A
NG_021311.2:g.22715A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.886T>A	ENSP00000365372.2:p.Phe296Ile
ENST00000376207.10:c.991T>A MANE Select	ENSP00000365380.4:p.Phe331Ile
ENST00000455775.7:c.1060T>A	ENSP00000396415.3:p.Phe354Ile
ENST00000518685.6:c.910T>A	ENSP00000428952.2:p.Phe304Ile
ENST00000557224.6:c.886T>A	ENSP00000451208.1:p.Phe296Ile
ENST00000651307.1:c.967+738T>A	ENSP00000498454.1:n.967+738T>A
ENST00000376197.1:c.841T>A	ENSP00000365369.1:p.Phe281Ile
ENST00000376199.6:c.886T>A	ENSP00000365372.2:p.Phe296Ile
ENST00000376207.8:c.991T>A	ENSP00000365380.4:p.Phe331Ile
ENST00000455775.6:c.1060T>A	ENSP00000396415.3:p.Phe354Ile
ENST00000518685.5:c.886T>A	ENSP00000428952.1:p.Phe296Ile
ENST00000557224.5:c.886T>A	ENSP00000451208.1:p.Phe296Ile
NM_001114377.1:c.886T>A	NP_001107849.1:p.Phe296Ile
NM_014009.3:c.991T>A , LRG_62t1:c.991T>A	NP_054728.2:p.Phe331Ile
XM_006724533.2:c.1060T>A	XP_006724596.2:p.Phe354Ile
XM_011543915.1:c.1210T>A	XP_011542217.1:p.Phe404Ile
XM_011543916.1:c.1210T>A	XP_011542218.1:p.Phe404Ile
XM_011543917.1:c.1009T>A	XP_011542219.1:p.Phe337Ile
XM_011543918.1:c.1246T>A	XP_011542220.1:p.Phe416Ile
XM_011543919.1:c.1210T>A	XP_011542221.1:p.Phe404Ile
XM_017029567.1:c.937T>A	XP_016885056.1:p.Phe313Ile
NM_001114377.2:c.886T>A	NP_001107849.1:p.Phe296Ile
NM_014009.4:c.991T>A MANE Select	NP_054728.2:p.Phe331Ile