Canonical Allele Identifier: CA2428552552

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255225_49255245delinsGCGTGAGCCACCACGCCCAGC , CM000685.2:g.49255225_49255245delinsGCGTGAGCCACCACGCCCAGC	GRCh38
NC_000023.10:g.49111686_49111706delinsGCGTGAGCCACCACGCCCAGC , CM000685.1:g.49111686_49111706delinsGCGTGAGCCACCACGCCCAGC	GRCh37
NC_000023.9:g.48998630_48998650delinsGCGTGAGCCACCACGCCCAGC	NCBI36
NG_007392.1:g.14583_14603delinsGCTGGGCGTGGTGGCTCACGC , LRG_62:g.14583_14603delinsGCTGGGCGTGGTGGCTCACGC
NG_021311.2:g.24761_24781delinsGCGTGAGCCACCACGCCCAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.711+184_711+204delinsGCTGGGCGTGGTGGCTCACGC	ENSP00000365372.2:n.711+184_711+204delinsGCTGGGCGTGGTGGCTCACG...
ENST00000376207.10:c.816+184_816+204delinsGCTGGGCGTGGTGGCTCACGC MANE Select	ENSP00000365380.4:n.816+184_816+204delinsGCTGGGCGTGGTGGCTCACG...
ENST00000455775.7:c.885+184_885+204delinsGCTGGGCGTGGTGGCTCACGC	ENSP00000396415.3:n.885+184_885+204delinsGCTGGGCGTGGTGGCTCACG...
ENST00000518685.6:c.735+470_735+490delinsGCTGGGCGTGGTGGCTCACGC	ENSP00000428952.2:n.735+470_735+490delinsGCTGGGCGTGGTGGCTCACG...
ENST00000557224.6:c.711+184_711+204delinsGCTGGGCGTGGTGGCTCACGC	ENSP00000451208.1:n.711+184_711+204delinsGCTGGGCGTGGTGGCTCACG...
ENST00000651307.1:c.816+184_816+204delinsGCTGGGCGTGGTGGCTCACGC	ENSP00000498454.1:n.816+184_816+204delinsGCTGGGCGTGGTGGCTCACG...
ENST00000376197.1:c.666+184_666+204delinsGCTGGGCGTGGTGGCTCACGC	ENSP00000365369.1:n.666+184_666+204delinsGCTGGGCGTGGTGGCTCACG...
ENST00000376199.6:c.711+184_711+204delinsGCTGGGCGTGGTGGCTCACGC	ENSP00000365372.2:n.711+184_711+204delinsGCTGGGCGTGGTGGCTCACG...
ENST00000376207.8:c.816+184_816+204delinsGCTGGGCGTGGTGGCTCACGC	ENSP00000365380.4:n.816+184_816+204delinsGCTGGGCGTGGTGGCTCACG...
ENST00000455775.6:c.885+184_885+204delinsGCTGGGCGTGGTGGCTCACGC	ENSP00000396415.3:n.885+184_885+204delinsGCTGGGCGTGGTGGCTCACG...
ENST00000518685.5:c.711+184_711+204delinsGCTGGGCGTGGTGGCTCACGC	ENSP00000428952.1:n.711+184_711+204delinsGCTGGGCGTGGTGGCTCACG...
ENST00000557224.5:c.711+184_711+204delinsGCTGGGCGTGGTGGCTCACGC	ENSP00000451208.1:n.711+184_711+204delinsGCTGGGCGTGGTGGCTCACG...
NM_001114377.1:c.711+184_711+204delinsGCTGGGCGTGGTGGCTCACGC	NP_001107849.1:n.711+184_711+204delinsGCTGGGCGTGGTGGCTCACGC
NM_014009.3:c.816+184_816+204delinsGCTGGGCGTGGTGGCTCACGC , LRG_62t1:c.816+184_816+204delinsGCTGGGCGTGGTGGCTCACGC	NP_054728.2:n.816+184_816+204delinsGCTGGGCGTGGTGGCTCACGC
XM_006724533.2:c.885+184_885+204delinsGCTGGGCGTGGTGGCTCACGC	XP_006724596.2:n.885+184_885+204delinsGCTGGGCGTGGTGGCTCACGC
XM_011543915.1:c.1035+184_1035+204delinsGCTGGGCGTGGTGGCTCACGC	XP_011542217.1:n.1035+184_1035+204delinsGCTGGGCGTGGTGGCTCACGC...
XM_011543916.1:c.1035+184_1035+204delinsGCTGGGCGTGGTGGCTCACGC	XP_011542218.1:n.1035+184_1035+204delinsGCTGGGCGTGGTGGCTCACGC...
XM_011543917.1:c.834+184_834+204delinsGCTGGGCGTGGTGGCTCACGC	XP_011542219.1:n.834+184_834+204delinsGCTGGGCGTGGTGGCTCACGC
XM_011543918.1:c.1071+184_1071+204delinsGCTGGGCGTGGTGGCTCACGC	XP_011542220.1:n.1071+184_1071+204delinsGCTGGGCGTGGTGGCTCACGC...
XM_011543919.1:c.1035+184_1035+204delinsGCTGGGCGTGGTGGCTCACGC	XP_011542221.1:n.1035+184_1035+204delinsGCTGGGCGTGGTGGCTCACGC...
XM_017029567.1:c.762+184_762+204delinsGCTGGGCGTGGTGGCTCACGC	XP_016885056.1:n.762+184_762+204delinsGCTGGGCGTGGTGGCTCACGC
NM_001114377.2:c.711+184_711+204delinsGCTGGGCGTGGTGGCTCACGC	NP_001107849.1:n.711+184_711+204delinsGCTGGGCGTGGTGGCTCACGC
NM_014009.4:c.816+184_816+204delinsGCTGGGCGTGGTGGCTCACGC MANE Select	NP_054728.2:n.816+184_816+204delinsGCTGGGCGTGGTGGCTCACGC