Canonical Allele Identifier: CA641903394

Gene: FOXP3

Linked Data

• dbSNP Id: rs1557116143
• gnomAD v2: X-49111878-G-A
• MyVariant Identifiers: chrX:g.49111878G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255417G>A , CM000685.2:g.49255417G>A	GRCh38
NC_000023.10:g.49111878G>A , CM000685.1:g.49111878G>A	GRCh37
NC_000023.9:g.48998822G>A	NCBI36
NG_007392.1:g.14411C>T , LRG_62:g.14411C>T
NG_021311.2:g.24953G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.711+12C>T	ENSP00000365372.2:n.711+12C>T
ENST00000376207.10:c.816+12C>T MANE Select	ENSP00000365380.4:n.816+12C>T
ENST00000455775.7:c.885+12C>T	ENSP00000396415.3:n.885+12C>T
ENST00000518685.6:c.735+298C>T	ENSP00000428952.2:n.735+298C>T
ENST00000557224.6:c.711+12C>T	ENSP00000451208.1:n.711+12C>T
ENST00000651307.1:c.816+12C>T	ENSP00000498454.1:n.816+12C>T
ENST00000376197.1:c.666+12C>T	ENSP00000365369.1:n.666+12C>T
ENST00000376199.6:c.711+12C>T	ENSP00000365372.2:n.711+12C>T
ENST00000376207.8:c.816+12C>T	ENSP00000365380.4:n.816+12C>T
ENST00000455775.6:c.885+12C>T	ENSP00000396415.3:n.885+12C>T
ENST00000518685.5:c.711+12C>T	ENSP00000428952.1:n.711+12C>T
ENST00000557224.5:c.711+12C>T	ENSP00000451208.1:n.711+12C>T
NM_001114377.1:c.711+12C>T	NP_001107849.1:n.711+12C>T
NM_014009.3:c.816+12C>T , LRG_62t1:c.816+12C>T	NP_054728.2:n.816+12C>T
XM_006724533.2:c.885+12C>T	XP_006724596.2:n.885+12C>T
XM_011543915.1:c.1035+12C>T	XP_011542217.1:n.1035+12C>T
XM_011543916.1:c.1035+12C>T	XP_011542218.1:n.1035+12C>T
XM_011543917.1:c.834+12C>T	XP_011542219.1:n.834+12C>T
XM_011543918.1:c.1071+12C>T	XP_011542220.1:n.1071+12C>T
XM_011543919.1:c.1035+12C>T	XP_011542221.1:n.1035+12C>T
XM_017029567.1:c.762+12C>T	XP_016885056.1:n.762+12C>T
NM_001114377.2:c.711+12C>T	NP_001107849.1:n.711+12C>T
NM_014009.4:c.816+12C>T MANE Select	NP_054728.2:n.816+12C>T