Canonical Allele Identifier: CA516397027

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49111902C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255441C>T , CM000685.2:g.49255441C>T	GRCh38
NC_000023.10:g.49111902C>T , CM000685.1:g.49111902C>T	GRCh37
NC_000023.9:g.48998846C>T	NCBI36
NG_007392.1:g.14387G>A , LRG_62:g.14387G>A
NG_021311.2:g.24977C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.699G>A	ENSP00000365372.2:p.Lys233=
ENST00000376207.10:c.804G>A MANE Select	ENSP00000365380.4:p.Lys268=
ENST00000455775.7:c.873G>A	ENSP00000396415.3:p.Lys291=
ENST00000518685.6:c.735+274G>A	ENSP00000428952.2:n.735+274G>A
ENST00000557224.6:c.699G>A	ENSP00000451208.1:p.Lys233=
ENST00000651307.1:c.804G>A	ENSP00000498454.1:p.Lys268=
ENST00000376197.1:c.654G>A	ENSP00000365369.1:p.Lys218=
ENST00000376199.6:c.699G>A	ENSP00000365372.2:p.Lys233=
ENST00000376207.8:c.804G>A	ENSP00000365380.4:p.Lys268=
ENST00000455775.6:c.873G>A	ENSP00000396415.3:p.Lys291=
ENST00000518685.5:c.699G>A	ENSP00000428952.1:p.Lys233=
ENST00000557224.5:c.699G>A	ENSP00000451208.1:p.Lys233=
NM_001114377.1:c.699G>A	NP_001107849.1:p.Lys233=
NM_014009.3:c.804G>A , LRG_62t1:c.804G>A	NP_054728.2:p.Lys268=
XM_006724533.2:c.873G>A	XP_006724596.2:p.Lys291=
XM_011543915.1:c.1023G>A	XP_011542217.1:p.Lys341=
XM_011543916.1:c.1023G>A	XP_011542218.1:p.Lys341=
XM_011543917.1:c.822G>A	XP_011542219.1:p.Lys274=
XM_011543918.1:c.1059G>A	XP_011542220.1:p.Lys353=
XM_011543919.1:c.1023G>A	XP_011542221.1:p.Lys341=
XM_017029567.1:c.750G>A	XP_016885056.1:p.Lys250=
NM_001114377.2:c.699G>A	NP_001107849.1:p.Lys233=
NM_014009.4:c.804G>A MANE Select	NP_054728.2:p.Lys268=