Canonical Allele Identifier: CA2693704833

Gene: FOXP3

Linked Data

• gnomAD v4: X-49255407-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255407C>A , CM000685.2:g.49255407C>A	GRCh38
NC_000023.10:g.49111868C>A , CM000685.1:g.49111868C>A	GRCh37
NC_000023.9:g.48998812C>A	NCBI36
NG_007392.1:g.14421G>T , LRG_62:g.14421G>T
NG_021311.2:g.24943C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.711+22G>T	ENSP00000365372.2:n.711+22G>T
ENST00000376207.10:c.816+22G>T MANE Select	ENSP00000365380.4:n.816+22G>T
ENST00000455775.7:c.885+22G>T	ENSP00000396415.3:n.885+22G>T
ENST00000518685.6:c.735+308G>T	ENSP00000428952.2:n.735+308G>T
ENST00000557224.6:c.711+22G>T	ENSP00000451208.1:n.711+22G>T
ENST00000651307.1:c.816+22G>T	ENSP00000498454.1:n.816+22G>T
ENST00000376197.1:c.666+22G>T	ENSP00000365369.1:n.666+22G>T
ENST00000376199.6:c.711+22G>T	ENSP00000365372.2:n.711+22G>T
ENST00000376207.8:c.816+22G>T	ENSP00000365380.4:n.816+22G>T
ENST00000455775.6:c.885+22G>T	ENSP00000396415.3:n.885+22G>T
ENST00000518685.5:c.711+22G>T	ENSP00000428952.1:n.711+22G>T
ENST00000557224.5:c.711+22G>T	ENSP00000451208.1:n.711+22G>T
NM_001114377.1:c.711+22G>T	NP_001107849.1:n.711+22G>T
NM_014009.3:c.816+22G>T , LRG_62t1:c.816+22G>T	NP_054728.2:n.816+22G>T
XM_006724533.2:c.885+22G>T	XP_006724596.2:n.885+22G>T
XM_011543915.1:c.1035+22G>T	XP_011542217.1:n.1035+22G>T
XM_011543916.1:c.1035+22G>T	XP_011542218.1:n.1035+22G>T
XM_011543917.1:c.834+22G>T	XP_011542219.1:n.834+22G>T
XM_011543918.1:c.1071+22G>T	XP_011542220.1:n.1071+22G>T
XM_011543919.1:c.1035+22G>T	XP_011542221.1:n.1035+22G>T
XM_017029567.1:c.762+22G>T	XP_016885056.1:n.762+22G>T
NM_001114377.2:c.711+22G>T	NP_001107849.1:n.711+22G>T
NM_014009.4:c.816+22G>T MANE Select	NP_054728.2:n.816+22G>T