Canonical Allele Identifier: CA412947596

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49107908A>C (hg19) ; chrX:g.49251447A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251447A>C , CM000685.2:g.49251447A>C	GRCh38
NC_000023.10:g.49107908A>C , CM000685.1:g.49107908A>C	GRCh37
NC_000023.9:g.48994852A>C	NCBI36
NG_007392.1:g.18381T>G , LRG_62:g.18381T>G
NG_021311.2:g.20983A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.1078T>G	ENSP00000365372.2:p.Phe360Val
ENST00000376207.10:c.1183T>G MANE Select	ENSP00000365380.4:p.Phe395Val
ENST00000455775.7:c.1252T>G	ENSP00000396415.3:p.Phe418Val
ENST00000518685.6:c.1102T>G	ENSP00000428952.2:p.Phe368Val
ENST00000557224.6:c.1258T>G	ENSP00000451208.1:p.Phe420Val
ENST00000651307.1:c.*98T>G	ENSP00000498454.1:n.*98T>G
ENST00000376197.1:c.1213T>G	ENSP00000365369.1:p.Phe405Val
ENST00000376199.6:c.1078T>G	ENSP00000365372.2:p.Phe360Val
ENST00000376207.8:c.1183T>G	ENSP00000365380.4:p.Phe395Val
ENST00000455775.6:c.1252T>G	ENSP00000396415.3:p.Phe418Val
ENST00000518685.5:c.1078T>G	ENSP00000428952.1:p.Phe360Val
ENST00000557224.5:c.1258T>G	ENSP00000451208.1:p.Phe420Val
NM_001114377.1:c.1078T>G	NP_001107849.1:p.Phe360Val
NM_014009.3:c.1183T>G , LRG_62t1:c.1183T>G	NP_054728.2:p.Phe395Val
XM_006724533.2:c.1252T>G	XP_006724596.2:p.Phe418Val
XM_011543915.1:c.1582T>G	XP_011542217.1:p.Phe528Val
XM_011543916.1:c.1582T>G	XP_011542218.1:p.Phe528Val
XM_011543917.1:c.1201T>G	XP_011542219.1:p.Phe401Val
XM_011543918.1:c.1438T>G	XP_011542220.1:p.Phe480Val
XM_011543919.1:c.1402T>G	XP_011542221.1:p.Phe468Val
XM_017029567.1:c.1309T>G	XP_016885056.1:p.Phe437Val
NM_001114377.2:c.1078T>G	NP_001107849.1:p.Phe360Val
NM_014009.4:c.1183T>G MANE Select	NP_054728.2:p.Phe395Val