Canonical Allele Identifier: CA412950953

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49111936T>A (hg19) ; chrX:g.49255475T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255475T>A , CM000685.2:g.49255475T>A	GRCh38
NC_000023.10:g.49111936T>A , CM000685.1:g.49111936T>A	GRCh37
NC_000023.9:g.48998880T>A	NCBI36
NG_007392.1:g.14353A>T , LRG_62:g.14353A>T
NG_021311.2:g.25011T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.665A>T	ENSP00000365372.2:p.Gln222Leu
ENST00000376207.10:c.770A>T MANE Select	ENSP00000365380.4:p.Gln257Leu
ENST00000455775.7:c.839A>T	ENSP00000396415.3:p.Gln280Leu
ENST00000518685.6:c.735+240A>T	ENSP00000428952.2:n.735+240A>T
ENST00000557224.6:c.665A>T	ENSP00000451208.1:p.Gln222Leu
ENST00000651307.1:c.770A>T	ENSP00000498454.1:p.Gln257Leu
ENST00000376197.1:c.620A>T	ENSP00000365369.1:p.Gln207Leu
ENST00000376199.6:c.665A>T	ENSP00000365372.2:p.Gln222Leu
ENST00000376207.8:c.770A>T	ENSP00000365380.4:p.Gln257Leu
ENST00000455775.6:c.839A>T	ENSP00000396415.3:p.Gln280Leu
ENST00000518685.5:c.665A>T	ENSP00000428952.1:p.Gln222Leu
ENST00000557224.5:c.665A>T	ENSP00000451208.1:p.Gln222Leu
NM_001114377.1:c.665A>T	NP_001107849.1:p.Gln222Leu
NM_014009.3:c.770A>T , LRG_62t1:c.770A>T	NP_054728.2:p.Gln257Leu
XM_006724533.2:c.839A>T	XP_006724596.2:p.Gln280Leu
XM_011543915.1:c.989A>T	XP_011542217.1:p.Gln330Leu
XM_011543916.1:c.989A>T	XP_011542218.1:p.Gln330Leu
XM_011543917.1:c.788A>T	XP_011542219.1:p.Gln263Leu
XM_011543918.1:c.1025A>T	XP_011542220.1:p.Gln342Leu
XM_011543919.1:c.989A>T	XP_011542221.1:p.Gln330Leu
XM_017029567.1:c.716A>T	XP_016885056.1:p.Gln239Leu
NM_001114377.2:c.665A>T	NP_001107849.1:p.Gln222Leu
NM_014009.4:c.770A>T MANE Select	NP_054728.2:p.Gln257Leu