Canonical Allele Identifier: CA2579609058

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255395_49255414del , CM000685.2:g.49255395_49255414del	GRCh38
NC_000023.10:g.49111856_49111875del , CM000685.1:g.49111856_49111875del	GRCh37
NC_000023.9:g.48998800_48998819del	NCBI36
NG_007392.1:g.14419_14438del , LRG_62:g.14419_14438del
NG_021311.2:g.24931_24950del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.711+20_711+39del	ENSP00000365372.2:n.711+20_711+39del
ENST00000376207.10:c.816+20_816+39del MANE Select	ENSP00000365380.4:n.816+20_816+39del
ENST00000455775.7:c.885+20_885+39del	ENSP00000396415.3:n.885+20_885+39del
ENST00000518685.6:c.735+306_735+325del	ENSP00000428952.2:n.735+306_735+325del
ENST00000557224.6:c.711+20_711+39del	ENSP00000451208.1:n.711+20_711+39del
ENST00000651307.1:c.816+20_816+39del	ENSP00000498454.1:n.816+20_816+39del
ENST00000376197.1:c.666+20_666+39del	ENSP00000365369.1:n.666+20_666+39del
ENST00000376199.6:c.711+20_711+39del	ENSP00000365372.2:n.711+20_711+39del
ENST00000376207.8:c.816+20_816+39del	ENSP00000365380.4:n.816+20_816+39del
ENST00000455775.6:c.885+20_885+39del	ENSP00000396415.3:n.885+20_885+39del
ENST00000518685.5:c.711+20_711+39del	ENSP00000428952.1:n.711+20_711+39del
ENST00000557224.5:c.711+20_711+39del	ENSP00000451208.1:n.711+20_711+39del
NM_001114377.1:c.711+20_711+39del	NP_001107849.1:n.711+20_711+39del
NM_014009.3:c.816+20_816+39del , LRG_62t1:c.816+20_816+39del	NP_054728.2:n.816+20_816+39del
XM_006724533.2:c.885+20_885+39del	XP_006724596.2:n.885+20_885+39del
XM_011543915.1:c.1035+20_1035+39del	XP_011542217.1:n.1035+20_1035+39del
XM_011543916.1:c.1035+20_1035+39del	XP_011542218.1:n.1035+20_1035+39del
XM_011543917.1:c.834+20_834+39del	XP_011542219.1:n.834+20_834+39del
XM_011543918.1:c.1071+20_1071+39del	XP_011542220.1:n.1071+20_1071+39del
XM_011543919.1:c.1035+20_1035+39del	XP_011542221.1:n.1035+20_1035+39del
XM_017029567.1:c.762+20_762+39del	XP_016885056.1:n.762+20_762+39del
NM_001114377.2:c.711+20_711+39del	NP_001107849.1:n.711+20_711+39del
NM_014009.4:c.816+20_816+39del MANE Select	NP_054728.2:n.816+20_816+39del