Canonical Allele Identifier: CA641903139

Gene: FOXP3

Linked Data

• dbSNP Id: rs1557115632
• gnomAD v2: X-49108242-TG-T
• gnomAD v4: X-49251781-TG-T
• MyVariant Identifiers: chrX:g.49108243del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251785del , CM000685.2:g.49251785del	GRCh38
NC_000023.10:g.49108246del , CM000685.1:g.49108246del	GRCh37
NC_000023.9:g.48995190del	NCBI36
NG_007392.1:g.18046del , LRG_62:g.18046del
NG_021311.2:g.21321del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.940-17del	ENSP00000365372.2:n.940-17del
ENST00000376207.10:c.1045-17del MANE Select	ENSP00000365380.4:n.1045-17del
ENST00000455775.7:c.1114-17del	ENSP00000396415.3:n.1114-17del
ENST00000518685.6:c.964-17del	ENSP00000428952.2:n.964-17del
ENST00000557224.6:c.940-17del	ENSP00000451208.1:n.940-17del
ENST00000651307.1:c.968-17del	ENSP00000498454.1:n.968-17del
ENST00000376197.1:c.895-17del	ENSP00000365369.1:n.895-17del
ENST00000376199.6:c.940-17del	ENSP00000365372.2:n.940-17del
ENST00000376207.8:c.1045-17del	ENSP00000365380.4:n.1045-17del
ENST00000455775.6:c.1114-17del	ENSP00000396415.3:n.1114-17del
ENST00000518685.5:c.940-17del	ENSP00000428952.1:n.940-17del
ENST00000557224.5:c.940-17del	ENSP00000451208.1:n.940-17del
NM_001114377.1:c.940-17del	NP_001107849.1:n.940-17del
NM_014009.3:c.1045-17del , LRG_62t1:c.1045-17del	NP_054728.2:n.1045-17del
XM_006724533.2:c.1114-17del	XP_006724596.2:n.1114-17del
XM_011543915.1:c.1264-17del	XP_011542217.1:n.1264-17del
XM_011543916.1:c.1264-17del	XP_011542218.1:n.1264-17del
XM_011543917.1:c.1063-17del	XP_011542219.1:n.1063-17del
XM_011543918.1:c.1300-17del	XP_011542220.1:n.1300-17del
XM_011543919.1:c.1264-17del	XP_011542221.1:n.1264-17del
XM_017029567.1:c.991-17del	XP_016885056.1:n.991-17del
NM_001114377.2:c.940-17del	NP_001107849.1:n.940-17del
NM_014009.4:c.1045-17del MANE Select	NP_054728.2:n.1045-17del