Canonical Allele Identifier: CA412948807

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108168G>A (hg19) ; chrX:g.49251707G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251707G>A , CM000685.2:g.49251707G>A	GRCh38
NC_000023.10:g.49108168G>A , CM000685.1:g.49108168G>A	GRCh37
NC_000023.9:g.48995112G>A	NCBI36
NG_007392.1:g.18121C>T , LRG_62:g.18121C>T
NG_021311.2:g.21243G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.998C>T	ENSP00000365372.2:p.Thr333Ile
ENST00000376207.10:c.1103C>T MANE Select	ENSP00000365380.4:p.Thr368Ile
ENST00000455775.7:c.1172C>T	ENSP00000396415.3:p.Thr391Ile
ENST00000518685.6:c.1022C>T	ENSP00000428952.2:p.Thr341Ile
ENST00000557224.6:c.998C>T	ENSP00000451208.1:p.Thr333Ile
ENST00000651307.1:c.*18C>T	ENSP00000498454.1:n.*18C>T
ENST00000376197.1:c.953C>T	ENSP00000365369.1:p.Thr318Ile
ENST00000376199.6:c.998C>T	ENSP00000365372.2:p.Thr333Ile
ENST00000376207.8:c.1103C>T	ENSP00000365380.4:p.Thr368Ile
ENST00000455775.6:c.1172C>T	ENSP00000396415.3:p.Thr391Ile
ENST00000518685.5:c.998C>T	ENSP00000428952.1:p.Thr333Ile
ENST00000557224.5:c.998C>T	ENSP00000451208.1:p.Thr333Ile
NM_001114377.1:c.998C>T	NP_001107849.1:p.Thr333Ile
NM_014009.3:c.1103C>T , LRG_62t1:c.1103C>T	NP_054728.2:p.Thr368Ile
XM_006724533.2:c.1172C>T	XP_006724596.2:p.Thr391Ile
XM_011543915.1:c.1322C>T	XP_011542217.1:p.Thr441Ile
XM_011543916.1:c.1322C>T	XP_011542218.1:p.Thr441Ile
XM_011543917.1:c.1121C>T	XP_011542219.1:p.Thr374Ile
XM_011543918.1:c.1358C>T	XP_011542220.1:p.Thr453Ile
XM_011543919.1:c.1322C>T	XP_011542221.1:p.Thr441Ile
XM_017029567.1:c.1049C>T	XP_016885056.1:p.Thr350Ile
NM_001114377.2:c.998C>T	NP_001107849.1:p.Thr333Ile
NM_014009.4:c.1103C>T MANE Select	NP_054728.2:p.Thr368Ile