Canonical Allele Identifier: CA412950257

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49109630T>C (hg19) ; chrX:g.49253169T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49253169T>C , CM000685.2:g.49253169T>C	GRCh38
NC_000023.10:g.49109630T>C , CM000685.1:g.49109630T>C	GRCh37
NC_000023.9:g.48996574T>C	NCBI36
NG_007392.1:g.16659A>G , LRG_62:g.16659A>G
NG_021311.2:g.22705T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.896A>G	ENSP00000365372.2:p.His299Arg
ENST00000376207.10:c.1001A>G MANE Select	ENSP00000365380.4:p.His334Arg
ENST00000455775.7:c.1070A>G	ENSP00000396415.3:p.His357Arg
ENST00000518685.6:c.920A>G	ENSP00000428952.2:p.His307Arg
ENST00000557224.6:c.896A>G	ENSP00000451208.1:p.His299Arg
ENST00000651307.1:c.967+748A>G	ENSP00000498454.1:n.967+748A>G
ENST00000376197.1:c.851A>G	ENSP00000365369.1:p.His284Arg
ENST00000376199.6:c.896A>G	ENSP00000365372.2:p.His299Arg
ENST00000376207.8:c.1001A>G	ENSP00000365380.4:p.His334Arg
ENST00000455775.6:c.1070A>G	ENSP00000396415.3:p.His357Arg
ENST00000518685.5:c.896A>G	ENSP00000428952.1:p.His299Arg
ENST00000557224.5:c.896A>G	ENSP00000451208.1:p.His299Arg
NM_001114377.1:c.896A>G	NP_001107849.1:p.His299Arg
NM_014009.3:c.1001A>G , LRG_62t1:c.1001A>G	NP_054728.2:p.His334Arg
XM_006724533.2:c.1070A>G	XP_006724596.2:p.His357Arg
XM_011543915.1:c.1220A>G	XP_011542217.1:p.His407Arg
XM_011543916.1:c.1220A>G	XP_011542218.1:p.His407Arg
XM_011543917.1:c.1019A>G	XP_011542219.1:p.His340Arg
XM_011543918.1:c.1256A>G	XP_011542220.1:p.His419Arg
XM_011543919.1:c.1220A>G	XP_011542221.1:p.His407Arg
XM_017029567.1:c.947A>G	XP_016885056.1:p.His316Arg
NM_001114377.2:c.896A>G	NP_001107849.1:p.His299Arg
NM_014009.4:c.1001A>G MANE Select	NP_054728.2:p.His334Arg