Canonical Allele Identifier: CA412951021

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49111963A>T (hg19) ; chrX:g.49255502A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255502A>T , CM000685.2:g.49255502A>T	GRCh38
NC_000023.10:g.49111963A>T , CM000685.1:g.49111963A>T	GRCh37
NC_000023.9:g.48998907A>T	NCBI36
NG_007392.1:g.14326T>A , LRG_62:g.14326T>A
NG_021311.2:g.25038A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.638T>A	ENSP00000365372.2:p.Leu213Gln
ENST00000376207.10:c.743T>A MANE Select	ENSP00000365380.4:p.Leu248Gln
ENST00000455775.7:c.812T>A	ENSP00000396415.3:p.Leu271Gln
ENST00000518685.6:c.735+213T>A	ENSP00000428952.2:n.735+213T>A
ENST00000557224.6:c.638T>A	ENSP00000451208.1:p.Leu213Gln
ENST00000651307.1:c.743T>A	ENSP00000498454.1:p.Leu248Gln
ENST00000376197.1:c.593T>A	ENSP00000365369.1:p.Leu198Gln
ENST00000376199.6:c.638T>A	ENSP00000365372.2:p.Leu213Gln
ENST00000376207.8:c.743T>A	ENSP00000365380.4:p.Leu248Gln
ENST00000455775.6:c.812T>A	ENSP00000396415.3:p.Leu271Gln
ENST00000518685.5:c.638T>A	ENSP00000428952.1:p.Leu213Gln
ENST00000557224.5:c.638T>A	ENSP00000451208.1:p.Leu213Gln
NM_001114377.1:c.638T>A	NP_001107849.1:p.Leu213Gln
NM_014009.3:c.743T>A , LRG_62t1:c.743T>A	NP_054728.2:p.Leu248Gln
XM_006724533.2:c.812T>A	XP_006724596.2:p.Leu271Gln
XM_011543915.1:c.962T>A	XP_011542217.1:p.Leu321Gln
XM_011543916.1:c.962T>A	XP_011542218.1:p.Leu321Gln
XM_011543917.1:c.761T>A	XP_011542219.1:p.Leu254Gln
XM_011543918.1:c.998T>A	XP_011542220.1:p.Leu333Gln
XM_011543919.1:c.962T>A	XP_011542221.1:p.Leu321Gln
XM_017029567.1:c.689T>A	XP_016885056.1:p.Leu230Gln
NM_001114377.2:c.638T>A	NP_001107849.1:p.Leu213Gln
NM_014009.4:c.743T>A MANE Select	NP_054728.2:p.Leu248Gln