Canonical Allele Identifier: CA516395849

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49109644G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49253183G>A , CM000685.2:g.49253183G>A	GRCh38
NC_000023.10:g.49109644G>A , CM000685.1:g.49109644G>A	GRCh37
NC_000023.9:g.48996588G>A	NCBI36
NG_007392.1:g.16645C>T , LRG_62:g.16645C>T
NG_021311.2:g.22719G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.882C>T	ENSP00000365372.2:p.Asp294=
ENST00000376207.10:c.987C>T MANE Select	ENSP00000365380.4:p.Asp329=
ENST00000455775.7:c.1056C>T	ENSP00000396415.3:p.Asp352=
ENST00000518685.6:c.906C>T	ENSP00000428952.2:p.Asp302=
ENST00000557224.6:c.882C>T	ENSP00000451208.1:p.Asp294=
ENST00000651307.1:c.967+734C>T	ENSP00000498454.1:n.967+734C>T
ENST00000376197.1:c.837C>T	ENSP00000365369.1:p.Asp279=
ENST00000376199.6:c.882C>T	ENSP00000365372.2:p.Asp294=
ENST00000376207.8:c.987C>T	ENSP00000365380.4:p.Asp329=
ENST00000455775.6:c.1056C>T	ENSP00000396415.3:p.Asp352=
ENST00000518685.5:c.882C>T	ENSP00000428952.1:p.Asp294=
ENST00000557224.5:c.882C>T	ENSP00000451208.1:p.Asp294=
NM_001114377.1:c.882C>T	NP_001107849.1:p.Asp294=
NM_014009.3:c.987C>T , LRG_62t1:c.987C>T	NP_054728.2:p.Asp329=
XM_006724533.2:c.1056C>T	XP_006724596.2:p.Asp352=
XM_011543915.1:c.1206C>T	XP_011542217.1:p.Asp402=
XM_011543916.1:c.1206C>T	XP_011542218.1:p.Asp402=
XM_011543917.1:c.1005C>T	XP_011542219.1:p.Asp335=
XM_011543918.1:c.1242C>T	XP_011542220.1:p.Asp414=
XM_011543919.1:c.1206C>T	XP_011542221.1:p.Asp402=
XM_017029567.1:c.933C>T	XP_016885056.1:p.Asp311=
NM_001114377.2:c.882C>T	NP_001107849.1:p.Asp294=
NM_014009.4:c.987C>T MANE Select	NP_054728.2:p.Asp329=