Canonical Allele Identifier: CA516397006

Gene: FOXP3

Linked Data

• gnomAD v4: X-49255432-A-G
• MyVariant Identifiers: chrX:g.49111893A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255432A>G , CM000685.2:g.49255432A>G	GRCh38
NC_000023.10:g.49111893A>G , CM000685.1:g.49111893A>G	GRCh37
NC_000023.9:g.48998837A>G	NCBI36
NG_007392.1:g.14396T>C , LRG_62:g.14396T>C
NG_021311.2:g.24968A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.708T>C	ENSP00000365372.2:p.Ser236=
ENST00000376207.10:c.813T>C MANE Select	ENSP00000365380.4:p.Ser271=
ENST00000455775.7:c.882T>C	ENSP00000396415.3:p.Ser294=
ENST00000518685.6:c.735+283T>C	ENSP00000428952.2:n.735+283T>C
ENST00000557224.6:c.708T>C	ENSP00000451208.1:p.Ser236=
ENST00000651307.1:c.813T>C	ENSP00000498454.1:p.Ser271=
ENST00000376197.1:c.663T>C	ENSP00000365369.1:p.Ser221=
ENST00000376199.6:c.708T>C	ENSP00000365372.2:p.Ser236=
ENST00000376207.8:c.813T>C	ENSP00000365380.4:p.Ser271=
ENST00000455775.6:c.882T>C	ENSP00000396415.3:p.Ser294=
ENST00000518685.5:c.708T>C	ENSP00000428952.1:p.Ser236=
ENST00000557224.5:c.708T>C	ENSP00000451208.1:p.Ser236=
NM_001114377.1:c.708T>C	NP_001107849.1:p.Ser236=
NM_014009.3:c.813T>C , LRG_62t1:c.813T>C	NP_054728.2:p.Ser271=
XM_006724533.2:c.882T>C	XP_006724596.2:p.Ser294=
XM_011543915.1:c.1032T>C	XP_011542217.1:p.Ser344=
XM_011543916.1:c.1032T>C	XP_011542218.1:p.Ser344=
XM_011543917.1:c.831T>C	XP_011542219.1:p.Ser277=
XM_011543918.1:c.1068T>C	XP_011542220.1:p.Ser356=
XM_011543919.1:c.1032T>C	XP_011542221.1:p.Ser344=
XM_017029567.1:c.759T>C	XP_016885056.1:p.Ser253=
NM_001114377.2:c.708T>C	NP_001107849.1:p.Ser236=
NM_014009.4:c.813T>C MANE Select	NP_054728.2:p.Ser271=