Canonical Allele Identifier: CA2428551832

Gene: FOXP3

Linked Data

• dbSNP Id: rs2066043821
• gnomAD v4: X-49252998-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49252998T>C , CM000685.2:g.49252998T>C	GRCh38
NC_000023.10:g.49109459T>C , CM000685.1:g.49109459T>C	GRCh37
NC_000023.9:g.48996403T>C	NCBI36
NG_007392.1:g.16830A>G , LRG_62:g.16830A>G
NG_021311.2:g.22534T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.939+128A>G	ENSP00000365372.2:n.939+128A>G
ENST00000376207.10:c.1044+128A>G MANE Select	ENSP00000365380.4:n.1044+128A>G
ENST00000455775.7:c.1113+128A>G	ENSP00000396415.3:n.1113+128A>G
ENST00000518685.6:c.963+128A>G	ENSP00000428952.2:n.963+128A>G
ENST00000557224.6:c.939+128A>G	ENSP00000451208.1:n.939+128A>G
ENST00000651307.1:c.967+919A>G	ENSP00000498454.1:n.967+919A>G
ENST00000376197.1:c.894+128A>G	ENSP00000365369.1:n.894+128A>G
ENST00000376199.6:c.939+128A>G	ENSP00000365372.2:n.939+128A>G
ENST00000376207.8:c.1044+128A>G	ENSP00000365380.4:n.1044+128A>G
ENST00000455775.6:c.1113+128A>G	ENSP00000396415.3:n.1113+128A>G
ENST00000518685.5:c.939+128A>G	ENSP00000428952.1:n.939+128A>G
ENST00000557224.5:c.939+128A>G	ENSP00000451208.1:n.939+128A>G
NM_001114377.1:c.939+128A>G	NP_001107849.1:n.939+128A>G
NM_014009.3:c.1044+128A>G , LRG_62t1:c.1044+128A>G	NP_054728.2:n.1044+128A>G
XM_006724533.2:c.1113+128A>G	XP_006724596.2:n.1113+128A>G
XM_011543915.1:c.1263+128A>G	XP_011542217.1:n.1263+128A>G
XM_011543916.1:c.1263+128A>G	XP_011542218.1:n.1263+128A>G
XM_011543917.1:c.1062+128A>G	XP_011542219.1:n.1062+128A>G
XM_011543918.1:c.1299+128A>G	XP_011542220.1:n.1299+128A>G
XM_011543919.1:c.1263+128A>G	XP_011542221.1:n.1263+128A>G
XM_017029567.1:c.990+128A>G	XP_016885056.1:n.990+128A>G
NM_001114377.2:c.939+128A>G	NP_001107849.1:n.939+128A>G
NM_014009.4:c.1044+128A>G MANE Select	NP_054728.2:n.1044+128A>G