Canonical Allele Identifier: CA412948986

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108210G>C (hg19) ; chrX:g.49251749G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251749G>C , CM000685.2:g.49251749G>C	GRCh38
NC_000023.10:g.49108210G>C , CM000685.1:g.49108210G>C	GRCh37
NC_000023.9:g.48995154G>C	NCBI36
NG_007392.1:g.18079C>G , LRG_62:g.18079C>G
NG_021311.2:g.21285G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.956C>G	ENSP00000365372.2:p.Pro319Arg
ENST00000376207.10:c.1061C>G MANE Select	ENSP00000365380.4:p.Pro354Arg
ENST00000455775.7:c.1130C>G	ENSP00000396415.3:p.Pro377Arg
ENST00000518685.6:c.980C>G	ENSP00000428952.2:p.Pro327Arg
ENST00000557224.6:c.956C>G	ENSP00000451208.1:p.Pro319Arg
ENST00000651307.1:c.984C>G	ENSP00000498454.1:p.Ser328=
ENST00000376197.1:c.911C>G	ENSP00000365369.1:p.Pro304Arg
ENST00000376199.6:c.956C>G	ENSP00000365372.2:p.Pro319Arg
ENST00000376207.8:c.1061C>G	ENSP00000365380.4:p.Pro354Arg
ENST00000455775.6:c.1130C>G	ENSP00000396415.3:p.Pro377Arg
ENST00000518685.5:c.956C>G	ENSP00000428952.1:p.Pro319Arg
ENST00000557224.5:c.956C>G	ENSP00000451208.1:p.Pro319Arg
NM_001114377.1:c.956C>G	NP_001107849.1:p.Pro319Arg
NM_014009.3:c.1061C>G , LRG_62t1:c.1061C>G	NP_054728.2:p.Pro354Arg
XM_006724533.2:c.1130C>G	XP_006724596.2:p.Pro377Arg
XM_011543915.1:c.1280C>G	XP_011542217.1:p.Pro427Arg
XM_011543916.1:c.1280C>G	XP_011542218.1:p.Pro427Arg
XM_011543917.1:c.1079C>G	XP_011542219.1:p.Pro360Arg
XM_011543918.1:c.1316C>G	XP_011542220.1:p.Pro439Arg
XM_011543919.1:c.1280C>G	XP_011542221.1:p.Pro427Arg
XM_017029567.1:c.1007C>G	XP_016885056.1:p.Pro336Arg
NM_001114377.2:c.956C>G	NP_001107849.1:p.Pro319Arg
NM_014009.4:c.1061C>G MANE Select	NP_054728.2:p.Pro354Arg