Canonical Allele Identifier: CA2428552652

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255526_49255527delinsAC , CM000685.2:g.49255526_49255527delinsAC	GRCh38
NC_000023.10:g.49111987_49111988delinsAC , CM000685.1:g.49111987_49111988delinsAC	GRCh37
NC_000023.9:g.48998931_48998932delinsAC	NCBI36
NG_007392.1:g.14301_14302delinsGT , LRG_62:g.14301_14302delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.631-18_631-17delinsGT	ENSP00000365372.2:n.631-18_631-17delinsGT
ENST00000376207.10:c.736-18_736-17delinsGT MANE Select	ENSP00000365380.4:n.736-18_736-17delinsGT
ENST00000455775.7:c.805-18_805-17delinsGT	ENSP00000396415.3:n.805-18_805-17delinsGT
ENST00000518685.6:c.735+188_735+189delinsGT	ENSP00000428952.2:n.735+188_735+189delinsGT
ENST00000557224.6:c.631-18_631-17delinsGT	ENSP00000451208.1:n.631-18_631-17delinsGT
ENST00000651307.1:c.736-18_736-17delinsGT	ENSP00000498454.1:n.736-18_736-17delinsGT
ENST00000376197.1:c.586-18_586-17delinsGT	ENSP00000365369.1:n.586-18_586-17delinsGT
ENST00000376199.6:c.631-18_631-17delinsGT	ENSP00000365372.2:n.631-18_631-17delinsGT
ENST00000376207.8:c.736-18_736-17delinsGT	ENSP00000365380.4:n.736-18_736-17delinsGT
ENST00000455775.6:c.805-18_805-17delinsGT	ENSP00000396415.3:n.805-18_805-17delinsGT
ENST00000518685.5:c.631-18_631-17delinsGT	ENSP00000428952.1:n.631-18_631-17delinsGT
ENST00000557224.5:c.631-18_631-17delinsGT	ENSP00000451208.1:n.631-18_631-17delinsGT
NM_001114377.1:c.631-18_631-17delinsGT	NP_001107849.1:n.631-18_631-17delinsGT
NM_014009.3:c.736-18_736-17delinsGT , LRG_62t1:c.736-18_736-17delinsGT	NP_054728.2:n.736-18_736-17delinsGT
XM_006724533.2:c.805-18_805-17delinsGT	XP_006724596.2:n.805-18_805-17delinsGT
XM_011543915.1:c.955-18_955-17delinsGT	XP_011542217.1:n.955-18_955-17delinsGT
XM_011543916.1:c.955-18_955-17delinsGT	XP_011542218.1:n.955-18_955-17delinsGT
XM_011543917.1:c.754-18_754-17delinsGT	XP_011542219.1:n.754-18_754-17delinsGT
XM_011543918.1:c.991-18_991-17delinsGT	XP_011542220.1:n.991-18_991-17delinsGT
XM_011543919.1:c.955-18_955-17delinsGT	XP_011542221.1:n.955-18_955-17delinsGT
XM_017029567.1:c.682-18_682-17delinsGT	XP_016885056.1:n.682-18_682-17delinsGT
NM_001114377.2:c.631-18_631-17delinsGT	NP_001107849.1:n.631-18_631-17delinsGT
NM_014009.4:c.736-18_736-17delinsGT MANE Select	NP_054728.2:n.736-18_736-17delinsGT