Canonical Allele Identifier: CA516569871

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108167T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251706T>C , CM000685.2:g.49251706T>C	GRCh38
NC_000023.10:g.49108167T>C , CM000685.1:g.49108167T>C	GRCh37
NC_000023.9:g.48995111T>C	NCBI36
NG_007392.1:g.18122A>G , LRG_62:g.18122A>G
NG_021311.2:g.21242T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.999A>G	ENSP00000365372.2:p.Thr333=
ENST00000376207.10:c.1104A>G MANE Select	ENSP00000365380.4:p.Thr368=
ENST00000455775.7:c.1173A>G	ENSP00000396415.3:p.Thr391=
ENST00000518685.6:c.1023A>G	ENSP00000428952.2:p.Thr341=
ENST00000557224.6:c.999A>G	ENSP00000451208.1:p.Thr333=
ENST00000651307.1:c.*19A>G	ENSP00000498454.1:n.*19A>G
ENST00000376197.1:c.954A>G	ENSP00000365369.1:p.Thr318=
ENST00000376199.6:c.999A>G	ENSP00000365372.2:p.Thr333=
ENST00000376207.8:c.1104A>G	ENSP00000365380.4:p.Thr368=
ENST00000455775.6:c.1173A>G	ENSP00000396415.3:p.Thr391=
ENST00000518685.5:c.999A>G	ENSP00000428952.1:p.Thr333=
ENST00000557224.5:c.999A>G	ENSP00000451208.1:p.Thr333=
NM_001114377.1:c.999A>G	NP_001107849.1:p.Thr333=
NM_014009.3:c.1104A>G , LRG_62t1:c.1104A>G	NP_054728.2:p.Thr368=
XM_006724533.2:c.1173A>G	XP_006724596.2:p.Thr391=
XM_011543915.1:c.1323A>G	XP_011542217.1:p.Thr441=
XM_011543916.1:c.1323A>G	XP_011542218.1:p.Thr441=
XM_011543917.1:c.1122A>G	XP_011542219.1:p.Thr374=
XM_011543918.1:c.1359A>G	XP_011542220.1:p.Thr453=
XM_011543919.1:c.1323A>G	XP_011542221.1:p.Thr441=
XM_017029567.1:c.1050A>G	XP_016885056.1:p.Thr350=
NM_001114377.2:c.999A>G	NP_001107849.1:p.Thr333=
NM_014009.4:c.1104A>G MANE Select	NP_054728.2:p.Thr368=