Canonical Allele Identifier: CA412950903

Gene: FOXP3

Linked Data

• gnomAD v4: X-49255452-C-T
• MyVariant Identifiers: chrX:g.49111913C>T (hg19) ; chrX:g.49255452C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255452C>T , CM000685.2:g.49255452C>T	GRCh38
NC_000023.10:g.49111913C>T , CM000685.1:g.49111913C>T	GRCh37
NC_000023.9:g.48998857C>T	NCBI36
NG_007392.1:g.14376G>A , LRG_62:g.14376G>A
NG_021311.2:g.24988C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.688G>A	ENSP00000365372.2:p.Ala230Thr
ENST00000376207.10:c.793G>A MANE Select	ENSP00000365380.4:p.Ala265Thr
ENST00000455775.7:c.862G>A	ENSP00000396415.3:p.Ala288Thr
ENST00000518685.6:c.735+263G>A	ENSP00000428952.2:n.735+263G>A
ENST00000557224.6:c.688G>A	ENSP00000451208.1:p.Ala230Thr
ENST00000651307.1:c.793G>A	ENSP00000498454.1:p.Ala265Thr
ENST00000376197.1:c.643G>A	ENSP00000365369.1:p.Ala215Thr
ENST00000376199.6:c.688G>A	ENSP00000365372.2:p.Ala230Thr
ENST00000376207.8:c.793G>A	ENSP00000365380.4:p.Ala265Thr
ENST00000455775.6:c.862G>A	ENSP00000396415.3:p.Ala288Thr
ENST00000518685.5:c.688G>A	ENSP00000428952.1:p.Ala230Thr
ENST00000557224.5:c.688G>A	ENSP00000451208.1:p.Ala230Thr
NM_001114377.1:c.688G>A	NP_001107849.1:p.Ala230Thr
NM_014009.3:c.793G>A , LRG_62t1:c.793G>A	NP_054728.2:p.Ala265Thr
XM_006724533.2:c.862G>A	XP_006724596.2:p.Ala288Thr
XM_011543915.1:c.1012G>A	XP_011542217.1:p.Ala338Thr
XM_011543916.1:c.1012G>A	XP_011542218.1:p.Ala338Thr
XM_011543917.1:c.811G>A	XP_011542219.1:p.Ala271Thr
XM_011543918.1:c.1048G>A	XP_011542220.1:p.Ala350Thr
XM_011543919.1:c.1012G>A	XP_011542221.1:p.Ala338Thr
XM_017029567.1:c.739G>A	XP_016885056.1:p.Ala247Thr
NM_001114377.2:c.688G>A	NP_001107849.1:p.Ala230Thr
NM_014009.4:c.793G>A MANE Select	NP_054728.2:p.Ala265Thr