Canonical Allele Identifier: CA412948946

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108196T>A (hg19) ; chrX:g.49251735T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251735T>A , CM000685.2:g.49251735T>A	GRCh38
NC_000023.10:g.49108196T>A , CM000685.1:g.49108196T>A	GRCh37
NC_000023.9:g.48995140T>A	NCBI36
NG_007392.1:g.18093A>T , LRG_62:g.18093A>T
NG_021311.2:g.21271T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.970A>T	ENSP00000365372.2:p.Thr324Ser
ENST00000376207.10:c.1075A>T MANE Select	ENSP00000365380.4:p.Thr359Ser
ENST00000455775.7:c.1144A>T	ENSP00000396415.3:p.Thr382Ser
ENST00000518685.6:c.994A>T	ENSP00000428952.2:p.Thr332Ser
ENST00000557224.6:c.970A>T	ENSP00000451208.1:p.Thr324Ser
ENST00000651307.1:c.998A>T	ENSP00000498454.1:p.Asp333Val
ENST00000376197.1:c.925A>T	ENSP00000365369.1:p.Thr309Ser
ENST00000376199.6:c.970A>T	ENSP00000365372.2:p.Thr324Ser
ENST00000376207.8:c.1075A>T	ENSP00000365380.4:p.Thr359Ser
ENST00000455775.6:c.1144A>T	ENSP00000396415.3:p.Thr382Ser
ENST00000518685.5:c.970A>T	ENSP00000428952.1:p.Thr324Ser
ENST00000557224.5:c.970A>T	ENSP00000451208.1:p.Thr324Ser
NM_001114377.1:c.970A>T	NP_001107849.1:p.Thr324Ser
NM_014009.3:c.1075A>T , LRG_62t1:c.1075A>T	NP_054728.2:p.Thr359Ser
XM_006724533.2:c.1144A>T	XP_006724596.2:p.Thr382Ser
XM_011543915.1:c.1294A>T	XP_011542217.1:p.Thr432Ser
XM_011543916.1:c.1294A>T	XP_011542218.1:p.Thr432Ser
XM_011543917.1:c.1093A>T	XP_011542219.1:p.Thr365Ser
XM_011543918.1:c.1330A>T	XP_011542220.1:p.Thr444Ser
XM_011543919.1:c.1294A>T	XP_011542221.1:p.Thr432Ser
XM_017029567.1:c.1021A>T	XP_016885056.1:p.Thr341Ser
NM_001114377.2:c.970A>T	NP_001107849.1:p.Thr324Ser
NM_014009.4:c.1075A>T MANE Select	NP_054728.2:p.Thr359Ser