Canonical Allele Identifier: CA16007744
Gene: FOXP3 HGNC NCBI

Linked Data

dbSNP Id: rs2280883
gnomAD v2: X-49109128-T-C
gnomAD v3: X-49252667-T-C
gnomAD v4: X-49252667-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49252667T>C , CM000685.2:g.49252667T>C GRCh38
NC_000023.10:g.49109128T>C , CM000685.1:g.49109128T>C GRCh37
NC_000023.9:g.48996072T>C NCBI36
NG_007392.1:g.17161A>G , LRG_62:g.17161A>G
NG_021311.2:g.22203T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376199.7:c.939+459A>G ENSP00000365372.2:n.939+459A>G
ENST00000376207.10:c.1044+459A>G MANE Select ENSP00000365380.4:n.1044+459A>G
ENST00000455775.7:c.1113+459A>G ENSP00000396415.3:n.1113+459A>G
ENST00000518685.6:c.963+459A>G ENSP00000428952.2:n.963+459A>G
ENST00000557224.6:c.939+459A>G ENSP00000451208.1:n.939+459A>G
ENST00000651307.1:c.968-902A>G ENSP00000498454.1:n.968-902A>G
ENST00000376197.1:c.894+459A>G ENSP00000365369.1:n.894+459A>G
ENST00000376199.6:c.939+459A>G ENSP00000365372.2:n.939+459A>G
ENST00000376207.8:c.1044+459A>G ENSP00000365380.4:n.1044+459A>G
ENST00000455775.6:c.1113+459A>G ENSP00000396415.3:n.1113+459A>G
ENST00000518685.5:c.939+459A>G ENSP00000428952.1:n.939+459A>G
ENST00000557224.5:c.939+459A>G ENSP00000451208.1:n.939+459A>G
NM_001114377.1:c.939+459A>G NP_001107849.1:n.939+459A>G
NM_014009.3:c.1044+459A>G , LRG_62t1:c.1044+459A>G NP_054728.2:n.1044+459A>G
XM_006724533.2:c.1113+459A>G XP_006724596.2:n.1113+459A>G
XM_011543915.1:c.1263+459A>G XP_011542217.1:n.1263+459A>G
XM_011543916.1:c.1263+459A>G XP_011542218.1:n.1263+459A>G
XM_011543917.1:c.1062+459A>G XP_011542219.1:n.1062+459A>G
XM_011543918.1:c.1299+459A>G XP_011542220.1:n.1299+459A>G
XM_011543919.1:c.1263+459A>G XP_011542221.1:n.1263+459A>G
XM_017029567.1:c.990+459A>G XP_016885056.1:n.990+459A>G
NM_001114377.2:c.939+459A>G NP_001107849.1:n.939+459A>G
NM_014009.4:c.1044+459A>G MANE Select NP_054728.2:n.1044+459A>G