Canonical Allele Identifier: CA412949047

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108225G>A (hg19) ; chrX:g.49251764G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251764G>A , CM000685.2:g.49251764G>A	GRCh38
NC_000023.10:g.49108225G>A , CM000685.1:g.49108225G>A	GRCh37
NC_000023.9:g.48995169G>A	NCBI36
NG_007392.1:g.18064C>T , LRG_62:g.18064C>T
NG_021311.2:g.21300G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.941C>T	ENSP00000365372.2:p.Ala314Val
ENST00000376207.10:c.1046C>T MANE Select	ENSP00000365380.4:p.Ala349Val
ENST00000455775.7:c.1115C>T	ENSP00000396415.3:p.Ala372Val
ENST00000518685.6:c.965C>T	ENSP00000428952.2:p.Ala322Val
ENST00000557224.6:c.941C>T	ENSP00000451208.1:p.Ala314Val
ENST00000651307.1:c.969C>T	ENSP00000498454.1:p.Gly323=
ENST00000376197.1:c.896C>T	ENSP00000365369.1:p.Ala299Val
ENST00000376199.6:c.941C>T	ENSP00000365372.2:p.Ala314Val
ENST00000376207.8:c.1046C>T	ENSP00000365380.4:p.Ala349Val
ENST00000455775.6:c.1115C>T	ENSP00000396415.3:p.Ala372Val
ENST00000518685.5:c.941C>T	ENSP00000428952.1:p.Ala314Val
ENST00000557224.5:c.941C>T	ENSP00000451208.1:p.Ala314Val
NM_001114377.1:c.941C>T	NP_001107849.1:p.Ala314Val
NM_014009.3:c.1046C>T , LRG_62t1:c.1046C>T	NP_054728.2:p.Ala349Val
XM_006724533.2:c.1115C>T	XP_006724596.2:p.Ala372Val
XM_011543915.1:c.1265C>T	XP_011542217.1:p.Ala422Val
XM_011543916.1:c.1265C>T	XP_011542218.1:p.Ala422Val
XM_011543917.1:c.1064C>T	XP_011542219.1:p.Ala355Val
XM_011543918.1:c.1301C>T	XP_011542220.1:p.Ala434Val
XM_011543919.1:c.1265C>T	XP_011542221.1:p.Ala422Val
XM_017029567.1:c.992C>T	XP_016885056.1:p.Ala331Val
NM_001114377.2:c.941C>T	NP_001107849.1:p.Ala314Val
NM_014009.4:c.1046C>T MANE Select	NP_054728.2:p.Ala349Val