Canonical Allele Identifier: CA412948810

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108169T>A (hg19) ; chrX:g.49251708T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251708T>A , CM000685.2:g.49251708T>A	GRCh38
NC_000023.10:g.49108169T>A , CM000685.1:g.49108169T>A	GRCh37
NC_000023.9:g.48995113T>A	NCBI36
NG_007392.1:g.18120A>T , LRG_62:g.18120A>T
NG_021311.2:g.21244T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.997A>T	ENSP00000365372.2:p.Thr333Ser
ENST00000376207.10:c.1102A>T MANE Select	ENSP00000365380.4:p.Thr368Ser
ENST00000455775.7:c.1171A>T	ENSP00000396415.3:p.Thr391Ser
ENST00000518685.6:c.1021A>T	ENSP00000428952.2:p.Thr341Ser
ENST00000557224.6:c.997A>T	ENSP00000451208.1:p.Thr333Ser
ENST00000651307.1:c.*17A>T	ENSP00000498454.1:n.*17A>T
ENST00000376197.1:c.952A>T	ENSP00000365369.1:p.Thr318Ser
ENST00000376199.6:c.997A>T	ENSP00000365372.2:p.Thr333Ser
ENST00000376207.8:c.1102A>T	ENSP00000365380.4:p.Thr368Ser
ENST00000455775.6:c.1171A>T	ENSP00000396415.3:p.Thr391Ser
ENST00000518685.5:c.997A>T	ENSP00000428952.1:p.Thr333Ser
ENST00000557224.5:c.997A>T	ENSP00000451208.1:p.Thr333Ser
NM_001114377.1:c.997A>T	NP_001107849.1:p.Thr333Ser
NM_014009.3:c.1102A>T , LRG_62t1:c.1102A>T	NP_054728.2:p.Thr368Ser
XM_006724533.2:c.1171A>T	XP_006724596.2:p.Thr391Ser
XM_011543915.1:c.1321A>T	XP_011542217.1:p.Thr441Ser
XM_011543916.1:c.1321A>T	XP_011542218.1:p.Thr441Ser
XM_011543917.1:c.1120A>T	XP_011542219.1:p.Thr374Ser
XM_011543918.1:c.1357A>T	XP_011542220.1:p.Thr453Ser
XM_011543919.1:c.1321A>T	XP_011542221.1:p.Thr441Ser
XM_017029567.1:c.1048A>T	XP_016885056.1:p.Thr350Ser
NM_001114377.2:c.997A>T	NP_001107849.1:p.Thr333Ser
NM_014009.4:c.1102A>T MANE Select	NP_054728.2:p.Thr368Ser