Canonical Allele Identifier: CA516395837

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49109638G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49253177G>A , CM000685.2:g.49253177G>A	GRCh38
NC_000023.10:g.49109638G>A , CM000685.1:g.49109638G>A	GRCh37
NC_000023.9:g.48996582G>A	NCBI36
NG_007392.1:g.16651C>T , LRG_62:g.16651C>T
NG_021311.2:g.22713G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.888C>T	ENSP00000365372.2:p.Phe296=
ENST00000376207.10:c.993C>T MANE Select	ENSP00000365380.4:p.Phe331=
ENST00000455775.7:c.1062C>T	ENSP00000396415.3:p.Phe354=
ENST00000518685.6:c.912C>T	ENSP00000428952.2:p.Phe304=
ENST00000557224.6:c.888C>T	ENSP00000451208.1:p.Phe296=
ENST00000651307.1:c.967+740C>T	ENSP00000498454.1:n.967+740C>T
ENST00000376197.1:c.843C>T	ENSP00000365369.1:p.Phe281=
ENST00000376199.6:c.888C>T	ENSP00000365372.2:p.Phe296=
ENST00000376207.8:c.993C>T	ENSP00000365380.4:p.Phe331=
ENST00000455775.6:c.1062C>T	ENSP00000396415.3:p.Phe354=
ENST00000518685.5:c.888C>T	ENSP00000428952.1:p.Phe296=
ENST00000557224.5:c.888C>T	ENSP00000451208.1:p.Phe296=
NM_001114377.1:c.888C>T	NP_001107849.1:p.Phe296=
NM_014009.3:c.993C>T , LRG_62t1:c.993C>T	NP_054728.2:p.Phe331=
XM_006724533.2:c.1062C>T	XP_006724596.2:p.Phe354=
XM_011543915.1:c.1212C>T	XP_011542217.1:p.Phe404=
XM_011543916.1:c.1212C>T	XP_011542218.1:p.Phe404=
XM_011543917.1:c.1011C>T	XP_011542219.1:p.Phe337=
XM_011543918.1:c.1248C>T	XP_011542220.1:p.Phe416=
XM_011543919.1:c.1212C>T	XP_011542221.1:p.Phe404=
XM_017029567.1:c.939C>T	XP_016885056.1:p.Phe313=
NM_001114377.2:c.888C>T	NP_001107849.1:p.Phe296=
NM_014009.4:c.993C>T MANE Select	NP_054728.2:p.Phe331=