Canonical Allele Identifier: CA516569889

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108199G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251738G>T , CM000685.2:g.49251738G>T	GRCh38
NC_000023.10:g.49108199G>T , CM000685.1:g.49108199G>T	GRCh37
NC_000023.9:g.48995143G>T	NCBI36
NG_007392.1:g.18090C>A , LRG_62:g.18090C>A
NG_021311.2:g.21274G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.967C>A	ENSP00000365372.2:p.Arg323=
ENST00000376207.10:c.1072C>A MANE Select	ENSP00000365380.4:p.Arg358=
ENST00000455775.7:c.1141C>A	ENSP00000396415.3:p.Arg381=
ENST00000518685.6:c.991C>A	ENSP00000428952.2:p.Arg331=
ENST00000557224.6:c.967C>A	ENSP00000451208.1:p.Arg323=
ENST00000651307.1:c.995C>A	ENSP00000498454.1:p.Ala332Glu
ENST00000376197.1:c.922C>A	ENSP00000365369.1:p.Arg308=
ENST00000376199.6:c.967C>A	ENSP00000365372.2:p.Arg323=
ENST00000376207.8:c.1072C>A	ENSP00000365380.4:p.Arg358=
ENST00000455775.6:c.1141C>A	ENSP00000396415.3:p.Arg381=
ENST00000518685.5:c.967C>A	ENSP00000428952.1:p.Arg323=
ENST00000557224.5:c.967C>A	ENSP00000451208.1:p.Arg323=
NM_001114377.1:c.967C>A	NP_001107849.1:p.Arg323=
NM_014009.3:c.1072C>A , LRG_62t1:c.1072C>A	NP_054728.2:p.Arg358=
XM_006724533.2:c.1141C>A	XP_006724596.2:p.Arg381=
XM_011543915.1:c.1291C>A	XP_011542217.1:p.Arg431=
XM_011543916.1:c.1291C>A	XP_011542218.1:p.Arg431=
XM_011543917.1:c.1090C>A	XP_011542219.1:p.Arg364=
XM_011543918.1:c.1327C>A	XP_011542220.1:p.Arg443=
XM_011543919.1:c.1291C>A	XP_011542221.1:p.Arg431=
XM_017029567.1:c.1018C>A	XP_016885056.1:p.Arg340=
NM_001114377.2:c.967C>A	NP_001107849.1:p.Arg323=
NM_014009.4:c.1072C>A MANE Select	NP_054728.2:p.Arg358=