Canonical Allele Identifier: CA412950956

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49111937G>T (hg19) ; chrX:g.49255476G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255476G>T , CM000685.2:g.49255476G>T	GRCh38
NC_000023.10:g.49111937G>T , CM000685.1:g.49111937G>T	GRCh37
NC_000023.9:g.48998881G>T	NCBI36
NG_007392.1:g.14352C>A , LRG_62:g.14352C>A
NG_021311.2:g.25012G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.664C>A	ENSP00000365372.2:p.Gln222Lys
ENST00000376207.10:c.769C>A MANE Select	ENSP00000365380.4:p.Gln257Lys
ENST00000455775.7:c.838C>A	ENSP00000396415.3:p.Gln280Lys
ENST00000518685.6:c.735+239C>A	ENSP00000428952.2:n.735+239C>A
ENST00000557224.6:c.664C>A	ENSP00000451208.1:p.Gln222Lys
ENST00000651307.1:c.769C>A	ENSP00000498454.1:p.Gln257Lys
ENST00000376197.1:c.619C>A	ENSP00000365369.1:p.Gln207Lys
ENST00000376199.6:c.664C>A	ENSP00000365372.2:p.Gln222Lys
ENST00000376207.8:c.769C>A	ENSP00000365380.4:p.Gln257Lys
ENST00000455775.6:c.838C>A	ENSP00000396415.3:p.Gln280Lys
ENST00000518685.5:c.664C>A	ENSP00000428952.1:p.Gln222Lys
ENST00000557224.5:c.664C>A	ENSP00000451208.1:p.Gln222Lys
NM_001114377.1:c.664C>A	NP_001107849.1:p.Gln222Lys
NM_014009.3:c.769C>A , LRG_62t1:c.769C>A	NP_054728.2:p.Gln257Lys
XM_006724533.2:c.838C>A	XP_006724596.2:p.Gln280Lys
XM_011543915.1:c.988C>A	XP_011542217.1:p.Gln330Lys
XM_011543916.1:c.988C>A	XP_011542218.1:p.Gln330Lys
XM_011543917.1:c.787C>A	XP_011542219.1:p.Gln263Lys
XM_011543918.1:c.1024C>A	XP_011542220.1:p.Gln342Lys
XM_011543919.1:c.988C>A	XP_011542221.1:p.Gln330Lys
XM_017029567.1:c.715C>A	XP_016885056.1:p.Gln239Lys
NM_001114377.2:c.664C>A	NP_001107849.1:p.Gln222Lys
NM_014009.4:c.769C>A MANE Select	NP_054728.2:p.Gln257Lys