Canonical Allele Identifier: CA412950871

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49111898A>C (hg19) ; chrX:g.49255437A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255437A>C , CM000685.2:g.49255437A>C	GRCh38
NC_000023.10:g.49111898A>C , CM000685.1:g.49111898A>C	GRCh37
NC_000023.9:g.48998842A>C	NCBI36
NG_007392.1:g.14391T>G , LRG_62:g.14391T>G
NG_021311.2:g.24973A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.703T>G	ENSP00000365372.2:p.Ser235Ala
ENST00000376207.10:c.808T>G MANE Select	ENSP00000365380.4:p.Ser270Ala
ENST00000455775.7:c.877T>G	ENSP00000396415.3:p.Ser293Ala
ENST00000518685.6:c.735+278T>G	ENSP00000428952.2:n.735+278T>G
ENST00000557224.6:c.703T>G	ENSP00000451208.1:p.Ser235Ala
ENST00000651307.1:c.808T>G	ENSP00000498454.1:p.Ser270Ala
ENST00000376197.1:c.658T>G	ENSP00000365369.1:p.Ser220Ala
ENST00000376199.6:c.703T>G	ENSP00000365372.2:p.Ser235Ala
ENST00000376207.8:c.808T>G	ENSP00000365380.4:p.Ser270Ala
ENST00000455775.6:c.877T>G	ENSP00000396415.3:p.Ser293Ala
ENST00000518685.5:c.703T>G	ENSP00000428952.1:p.Ser235Ala
ENST00000557224.5:c.703T>G	ENSP00000451208.1:p.Ser235Ala
NM_001114377.1:c.703T>G	NP_001107849.1:p.Ser235Ala
NM_014009.3:c.808T>G , LRG_62t1:c.808T>G	NP_054728.2:p.Ser270Ala
XM_006724533.2:c.877T>G	XP_006724596.2:p.Ser293Ala
XM_011543915.1:c.1027T>G	XP_011542217.1:p.Ser343Ala
XM_011543916.1:c.1027T>G	XP_011542218.1:p.Ser343Ala
XM_011543917.1:c.826T>G	XP_011542219.1:p.Ser276Ala
XM_011543918.1:c.1063T>G	XP_011542220.1:p.Ser355Ala
XM_011543919.1:c.1027T>G	XP_011542221.1:p.Ser343Ala
XM_017029567.1:c.754T>G	XP_016885056.1:p.Ser252Ala
NM_001114377.2:c.703T>G	NP_001107849.1:p.Ser235Ala
NM_014009.4:c.808T>G MANE Select	NP_054728.2:p.Ser270Ala