Canonical Allele Identifier: CA516569902

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108221G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251760G>A , CM000685.2:g.49251760G>A	GRCh38
NC_000023.10:g.49108221G>A , CM000685.1:g.49108221G>A	GRCh37
NC_000023.9:g.48995165G>A	NCBI36
NG_007392.1:g.18068C>T , LRG_62:g.18068C>T
NG_021311.2:g.21296G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.945C>T	ENSP00000365372.2:p.Ile315=
ENST00000376207.10:c.1050C>T MANE Select	ENSP00000365380.4:p.Ile350=
ENST00000455775.7:c.1119C>T	ENSP00000396415.3:p.Ile373=
ENST00000518685.6:c.969C>T	ENSP00000428952.2:p.Ile323=
ENST00000557224.6:c.945C>T	ENSP00000451208.1:p.Ile315=
ENST00000651307.1:c.973C>T	ENSP00000498454.1:p.Pro325Ser
ENST00000376197.1:c.900C>T	ENSP00000365369.1:p.Ile300=
ENST00000376199.6:c.945C>T	ENSP00000365372.2:p.Ile315=
ENST00000376207.8:c.1050C>T	ENSP00000365380.4:p.Ile350=
ENST00000455775.6:c.1119C>T	ENSP00000396415.3:p.Ile373=
ENST00000518685.5:c.945C>T	ENSP00000428952.1:p.Ile315=
ENST00000557224.5:c.945C>T	ENSP00000451208.1:p.Ile315=
NM_001114377.1:c.945C>T	NP_001107849.1:p.Ile315=
NM_014009.3:c.1050C>T , LRG_62t1:c.1050C>T	NP_054728.2:p.Ile350=
XM_006724533.2:c.1119C>T	XP_006724596.2:p.Ile373=
XM_011543915.1:c.1269C>T	XP_011542217.1:p.Ile423=
XM_011543916.1:c.1269C>T	XP_011542218.1:p.Ile423=
XM_011543917.1:c.1068C>T	XP_011542219.1:p.Ile356=
XM_011543918.1:c.1305C>T	XP_011542220.1:p.Ile435=
XM_011543919.1:c.1269C>T	XP_011542221.1:p.Ile423=
XM_017029567.1:c.996C>T	XP_016885056.1:p.Ile332=
NM_001114377.2:c.945C>T	NP_001107849.1:p.Ile315=
NM_014009.4:c.1050C>T MANE Select	NP_054728.2:p.Ile350=