Canonical Allele Identifier: CA875957688

Gene: FOXP3

Linked Data

• dbSNP Id: rs1479209953
• MyVariant Identifiers: chrX:g.49251779_49251781del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251781_49251783del , CM000685.2:g.49251781_49251783del	GRCh38
NC_000023.10:g.49108242_49108244del , CM000685.1:g.49108242_49108244del	GRCh37
NC_000023.9:g.48995186_48995188del	NCBI36
NG_007392.1:g.18047_18049del , LRG_62:g.18047_18049del
NG_021311.2:g.21317_21319del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.940-16_940-14del	ENSP00000365372.2:n.940-16_940-14del
ENST00000376207.10:c.1045-16_1045-14del MANE Select	ENSP00000365380.4:n.1045-16_1045-14del
ENST00000455775.7:c.1114-16_1114-14del	ENSP00000396415.3:n.1114-16_1114-14del
ENST00000518685.6:c.964-16_964-14del	ENSP00000428952.2:n.964-16_964-14del
ENST00000557224.6:c.940-16_940-14del	ENSP00000451208.1:n.940-16_940-14del
ENST00000651307.1:c.968-16_968-14del	ENSP00000498454.1:n.968-16_968-14del
ENST00000376197.1:c.895-16_895-14del	ENSP00000365369.1:n.895-16_895-14del
ENST00000376199.6:c.940-16_940-14del	ENSP00000365372.2:n.940-16_940-14del
ENST00000376207.8:c.1045-16_1045-14del	ENSP00000365380.4:n.1045-16_1045-14del
ENST00000455775.6:c.1114-16_1114-14del	ENSP00000396415.3:n.1114-16_1114-14del
ENST00000518685.5:c.940-16_940-14del	ENSP00000428952.1:n.940-16_940-14del
ENST00000557224.5:c.940-16_940-14del	ENSP00000451208.1:n.940-16_940-14del
NM_001114377.1:c.940-16_940-14del	NP_001107849.1:n.940-16_940-14del
NM_014009.3:c.1045-16_1045-14del , LRG_62t1:c.1045-16_1045-14del	NP_054728.2:n.1045-16_1045-14del
XM_006724533.2:c.1114-16_1114-14del	XP_006724596.2:n.1114-16_1114-14del
XM_011543915.1:c.1264-16_1264-14del	XP_011542217.1:n.1264-16_1264-14del
XM_011543916.1:c.1264-16_1264-14del	XP_011542218.1:n.1264-16_1264-14del
XM_011543917.1:c.1063-16_1063-14del	XP_011542219.1:n.1063-16_1063-14del
XM_011543918.1:c.1300-16_1300-14del	XP_011542220.1:n.1300-16_1300-14del
XM_011543919.1:c.1264-16_1264-14del	XP_011542221.1:n.1264-16_1264-14del
XM_017029567.1:c.991-16_991-14del	XP_016885056.1:n.991-16_991-14del
NM_001114377.2:c.940-16_940-14del	NP_001107849.1:n.940-16_940-14del
NM_014009.4:c.1045-16_1045-14del MANE Select	NP_054728.2:n.1045-16_1045-14del