Canonical Allele Identifier: CA10411675

Gene: FOXP3

Linked Data

• dbSNP Id: rs782289093
• ExAC: X:49108272 G / GT
• gnomAD v2: X-49108272-G-GT
• gnomAD v3: X-49251811-G-GT
• gnomAD v4: X-49251811-G-GT
• MyVariant Identifiers: chrX:g.49108272_49108273insT (hg19) ; chrX:g.49251811_49251812insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251811_49251812insT , CM000685.2:g.49251811_49251812insT	GRCh38
NC_000023.10:g.49108272_49108273insT , CM000685.1:g.49108272_49108273insT	GRCh37
NC_000023.9:g.48995216_48995217insT	NCBI36
NG_007392.1:g.18016_18017insA , LRG_62:g.18016_18017insA
NG_021311.2:g.21347_21348insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.940-47_940-46insA	ENSP00000365372.2:n.940-47_940-46insA
ENST00000376207.10:c.1045-47_1045-46insA MANE Select	ENSP00000365380.4:n.1045-47_1045-46insA
ENST00000455775.7:c.1114-47_1114-46insA	ENSP00000396415.3:n.1114-47_1114-46insA
ENST00000518685.6:c.964-47_964-46insA	ENSP00000428952.2:n.964-47_964-46insA
ENST00000557224.6:c.940-47_940-46insA	ENSP00000451208.1:n.940-47_940-46insA
ENST00000651307.1:c.968-47_968-46insA	ENSP00000498454.1:n.968-47_968-46insA
ENST00000376197.1:c.895-47_895-46insA	ENSP00000365369.1:n.895-47_895-46insA
ENST00000376199.6:c.940-47_940-46insA	ENSP00000365372.2:n.940-47_940-46insA
ENST00000376207.8:c.1045-47_1045-46insA	ENSP00000365380.4:n.1045-47_1045-46insA
ENST00000455775.6:c.1114-47_1114-46insA	ENSP00000396415.3:n.1114-47_1114-46insA
ENST00000518685.5:c.940-47_940-46insA	ENSP00000428952.1:n.940-47_940-46insA
ENST00000557224.5:c.940-47_940-46insA	ENSP00000451208.1:n.940-47_940-46insA
NM_001114377.1:c.940-47_940-46insA	NP_001107849.1:n.940-47_940-46insA
NM_014009.3:c.1045-47_1045-46insA , LRG_62t1:c.1045-47_1045-46insA	NP_054728.2:n.1045-47_1045-46insA
XM_006724533.2:c.1114-47_1114-46insA	XP_006724596.2:n.1114-47_1114-46insA
XM_011543915.1:c.1264-47_1264-46insA	XP_011542217.1:n.1264-47_1264-46insA
XM_011543916.1:c.1264-47_1264-46insA	XP_011542218.1:n.1264-47_1264-46insA
XM_011543917.1:c.1063-47_1063-46insA	XP_011542219.1:n.1063-47_1063-46insA
XM_011543918.1:c.1300-47_1300-46insA	XP_011542220.1:n.1300-47_1300-46insA
XM_011543919.1:c.1264-47_1264-46insA	XP_011542221.1:n.1264-47_1264-46insA
XM_017029567.1:c.991-47_991-46insA	XP_016885056.1:n.991-47_991-46insA
NM_001114377.2:c.940-47_940-46insA	NP_001107849.1:n.940-47_940-46insA
NM_014009.4:c.1045-47_1045-46insA MANE Select	NP_054728.2:n.1045-47_1045-46insA