Canonical Allele Identifier: CA516569904

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108224G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251763G>A , CM000685.2:g.49251763G>A	GRCh38
NC_000023.10:g.49108224G>A , CM000685.1:g.49108224G>A	GRCh37
NC_000023.9:g.48995168G>A	NCBI36
NG_007392.1:g.18065C>T , LRG_62:g.18065C>T
NG_021311.2:g.21299G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.942C>T	ENSP00000365372.2:p.Ala314=
ENST00000376207.10:c.1047C>T MANE Select	ENSP00000365380.4:p.Ala349=
ENST00000455775.7:c.1116C>T	ENSP00000396415.3:p.Ala372=
ENST00000518685.6:c.966C>T	ENSP00000428952.2:p.Ala322=
ENST00000557224.6:c.942C>T	ENSP00000451208.1:p.Ala314=
ENST00000651307.1:c.970C>T	ENSP00000498454.1:p.His324Tyr
ENST00000376197.1:c.897C>T	ENSP00000365369.1:p.Ala299=
ENST00000376199.6:c.942C>T	ENSP00000365372.2:p.Ala314=
ENST00000376207.8:c.1047C>T	ENSP00000365380.4:p.Ala349=
ENST00000455775.6:c.1116C>T	ENSP00000396415.3:p.Ala372=
ENST00000518685.5:c.942C>T	ENSP00000428952.1:p.Ala314=
ENST00000557224.5:c.942C>T	ENSP00000451208.1:p.Ala314=
NM_001114377.1:c.942C>T	NP_001107849.1:p.Ala314=
NM_014009.3:c.1047C>T , LRG_62t1:c.1047C>T	NP_054728.2:p.Ala349=
XM_006724533.2:c.1116C>T	XP_006724596.2:p.Ala372=
XM_011543915.1:c.1266C>T	XP_011542217.1:p.Ala422=
XM_011543916.1:c.1266C>T	XP_011542218.1:p.Ala422=
XM_011543917.1:c.1065C>T	XP_011542219.1:p.Ala355=
XM_011543918.1:c.1302C>T	XP_011542220.1:p.Ala434=
XM_011543919.1:c.1266C>T	XP_011542221.1:p.Ala422=
XM_017029567.1:c.993C>T	XP_016885056.1:p.Ala331=
NM_001114377.2:c.942C>T	NP_001107849.1:p.Ala314=
NM_014009.4:c.1047C>T MANE Select	NP_054728.2:p.Ala349=