Canonical Allele Identifier: CA516399644

Gene: FOXP3

Linked Data

• gnomAD v4: X-49258389-C-T
• MyVariant Identifiers: chrX:g.49114846C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49258389C>T , CM000685.2:g.49258389C>T	GRCh38
NC_000023.10:g.49114846C>T , CM000685.1:g.49114846C>T	GRCh37
NC_000023.9:g.49001790C>T	NCBI36
NG_007392.1:g.11443G>A , LRG_62:g.11443G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703450.1:c.117G>A	ENSP00000515301.1:p.Arg39=
ENST00000684155.1:c.117G>A	ENSP00000507726.1:p.Arg39=
ENST00000376199.7:c.117G>A	ENSP00000365372.2:p.Arg39=
ENST00000376207.10:c.117G>A MANE Select	ENSP00000365380.4:p.Arg39=
ENST00000455775.7:c.117G>A	ENSP00000396415.3:p.Arg39=
ENST00000518685.6:c.117G>A	ENSP00000428952.2:p.Arg39=
ENST00000557224.6:c.117G>A	ENSP00000451208.1:p.Arg39=
ENST00000650877.1:c.117G>A	ENSP00000499100.1:p.Arg39=
ENST00000651307.1:c.117G>A	ENSP00000498454.1:p.Arg39=
ENST00000652559.1:c.117G>A	ENSP00000498236.1:p.Arg39=
ENST00000376197.1:c.72G>A	ENSP00000365369.1:p.Arg24=
ENST00000376199.6:c.117G>A	ENSP00000365372.2:p.Arg39=
ENST00000376207.8:c.117G>A	ENSP00000365380.4:p.Arg39=
ENST00000455775.6:c.117G>A	ENSP00000396415.3:p.Arg39=
ENST00000518685.5:c.117G>A	ENSP00000428952.1:p.Arg39=
ENST00000557224.5:c.117G>A	ENSP00000451208.1:p.Arg39=
NM_001114377.1:c.117G>A	NP_001107849.1:p.Arg39=
NM_014009.3:c.117G>A , LRG_62t1:c.117G>A	NP_054728.2:p.Arg39=
XM_006724533.2:c.117G>A	XP_006724596.2:p.Arg39=
XM_011543915.1:c.441G>A	XP_011542217.1:p.Arg147=
XM_011543916.1:c.441G>A	XP_011542218.1:p.Arg147=
XM_011543917.1:c.117G>A	XP_011542219.1:p.Arg39=
XM_011543918.1:c.441G>A	XP_011542220.1:p.Arg147=
XM_011543919.1:c.441G>A	XP_011542221.1:p.Arg147=
XM_017029567.1:c.168G>A	XP_016885056.1:p.Arg56=
NM_001114377.2:c.117G>A	NP_001107849.1:p.Arg39=
NM_014009.4:c.117G>A MANE Select	NP_054728.2:p.Arg39=