Canonical Allele Identifier: CA412953354

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49257682C>A , CM000685.2:g.49257682C>A	GRCh38
NC_000023.10:g.49114139C>A , CM000685.1:g.49114139C>A	GRCh37
NC_000023.9:g.49001083C>A	NCBI36
NG_007392.1:g.12150G>T , LRG_62:g.12150G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014009.4:c.297G>T MANE Select	NP_054728.2:p.Arg99Ser
ENST00000376207.10:c.297G>T MANE Select	ENSP00000365380.4:p.Arg99Ser
NM_001114377.1:c.211-117G>T	NP_001107849.1:n.211-117G>T
NM_001114377.2:c.211-117G>T	NP_001107849.1:n.211-117G>T
NM_014009.3:c.297G>T , LRG_62t1:c.297G>T	NP_054728.2:p.Arg99Ser
ENST00000376197.1:c.166-117G>T	ENSP00000365369.1:n.166-117G>T
ENST00000376199.6:c.211-117G>T	ENSP00000365372.2:n.211-117G>T
ENST00000376199.7:c.211-117G>T	ENSP00000365372.2:n.211-117G>T
ENST00000376207.8:c.297G>T	ENSP00000365380.4:p.Arg99Ser
ENST00000455775.6:c.297G>T	ENSP00000396415.3:p.Arg99Ser
ENST00000455775.7:c.297G>T	ENSP00000396415.3:p.Arg99Ser
ENST00000518685.5:c.211-117G>T	ENSP00000428952.1:n.211-117G>T
ENST00000518685.6:c.297G>T	ENSP00000428952.2:p.Arg99Ser
ENST00000557224.5:c.211-117G>T	ENSP00000451208.1:n.211-117G>T
ENST00000557224.6:c.211-117G>T	ENSP00000451208.1:n.211-117G>T
ENST00000651307.1:c.297G>T	ENSP00000498454.1:p.Arg99Ser
ENST00000652559.1:c.211-159G>T	ENSP00000498236.1:n.211-159G>T
ENST00000684155.1:c.228G>T	ENSP00000507726.1:p.Arg76Ser
XM_006724533.2:c.297G>T	XP_006724596.2:p.Arg99Ser
XM_011543915.1:c.535-117G>T	XP_011542217.1:n.535-117G>T
XM_011543916.1:c.535-117G>T	XP_011542218.1:n.535-117G>T
XM_011543917.1:c.297G>T	XP_011542219.1:p.Arg99Ser
XM_011543918.1:c.552G>T	XP_011542220.1:p.Arg184Ser
XM_011543919.1:c.535-117G>T	XP_011542221.1:n.535-117G>T
XM_017029567.1:c.262-117G>T	XP_016885056.1:n.262-117G>T