Canonical Allele Identifier: CA516397207

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49111959C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255498C>T , CM000685.2:g.49255498C>T	GRCh38
NC_000023.10:g.49111959C>T , CM000685.1:g.49111959C>T	GRCh37
NC_000023.9:g.48998903C>T	NCBI36
NG_007392.1:g.14330G>A , LRG_62:g.14330G>A
NG_021311.2:g.25034C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.642G>A	ENSP00000365372.2:p.Glu214=
ENST00000376207.10:c.747G>A MANE Select	ENSP00000365380.4:p.Glu249=
ENST00000455775.7:c.816G>A	ENSP00000396415.3:p.Glu272=
ENST00000518685.6:c.735+217G>A	ENSP00000428952.2:n.735+217G>A
ENST00000557224.6:c.642G>A	ENSP00000451208.1:p.Glu214=
ENST00000651307.1:c.747G>A	ENSP00000498454.1:p.Glu249=
ENST00000376197.1:c.597G>A	ENSP00000365369.1:p.Glu199=
ENST00000376199.6:c.642G>A	ENSP00000365372.2:p.Glu214=
ENST00000376207.8:c.747G>A	ENSP00000365380.4:p.Glu249=
ENST00000455775.6:c.816G>A	ENSP00000396415.3:p.Glu272=
ENST00000518685.5:c.642G>A	ENSP00000428952.1:p.Glu214=
ENST00000557224.5:c.642G>A	ENSP00000451208.1:p.Glu214=
NM_001114377.1:c.642G>A	NP_001107849.1:p.Glu214=
NM_014009.3:c.747G>A , LRG_62t1:c.747G>A	NP_054728.2:p.Glu249=
XM_006724533.2:c.816G>A	XP_006724596.2:p.Glu272=
XM_011543915.1:c.966G>A	XP_011542217.1:p.Glu322=
XM_011543916.1:c.966G>A	XP_011542218.1:p.Glu322=
XM_011543917.1:c.765G>A	XP_011542219.1:p.Glu255=
XM_011543918.1:c.1002G>A	XP_011542220.1:p.Glu334=
XM_011543919.1:c.966G>A	XP_011542221.1:p.Glu322=
XM_017029567.1:c.693G>A	XP_016885056.1:p.Glu231=
NM_001114377.2:c.642G>A	NP_001107849.1:p.Glu214=
NM_014009.4:c.747G>A MANE Select	NP_054728.2:p.Glu249=