Canonical Allele Identifier: CA412947071

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251359C>T , CM000685.2:g.49251359C>T	GRCh38
NC_000023.10:g.49107820C>T , CM000685.1:g.49107820C>T	GRCh37
NC_000023.9:g.48994764C>T	NCBI36
NG_007392.1:g.18469G>A , LRG_62:g.18469G>A
NG_021311.2:g.20895C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014009.4:c.1271G>A MANE Select	NP_054728.2:p.Cys424Tyr
ENST00000376207.10:c.1271G>A MANE Select	ENSP00000365380.4:p.Cys424Tyr
NM_001114377.1:c.1166G>A	NP_001107849.1:p.Cys389Tyr
NM_001114377.2:c.1166G>A	NP_001107849.1:p.Cys389Tyr
NM_014009.3:c.1271G>A , LRG_62t1:c.1271G>A	NP_054728.2:p.Cys424Tyr
ENST00000376197.1:c.1301G>A	ENSP00000365369.1:p.Cys434Tyr
ENST00000376199.6:c.1166G>A	ENSP00000365372.2:p.Cys389Tyr
ENST00000376199.7:c.1166G>A	ENSP00000365372.2:p.Cys389Tyr
ENST00000376207.8:c.1271G>A	ENSP00000365380.4:p.Cys424Tyr
ENST00000455775.6:c.1340G>A	ENSP00000396415.3:p.Cys447Tyr
ENST00000455775.7:c.1340G>A	ENSP00000396415.3:p.Cys447Tyr
ENST00000518685.5:c.1166G>A	ENSP00000428952.1:p.Cys389Tyr
ENST00000518685.6:c.1190G>A	ENSP00000428952.2:p.Cys397Tyr
ENST00000557224.5:c.1346G>A	ENSP00000451208.1:p.Cys449Tyr
ENST00000557224.6:c.1346G>A	ENSP00000451208.1:p.Cys449Tyr
ENST00000651307.1:c.*186G>A	ENSP00000498454.1:n.*186G>A
XM_006724533.2:c.1340G>A	XP_006724596.2:p.Cys447Tyr
XM_011543915.1:c.1670G>A	XP_011542217.1:p.Cys557Tyr
XM_011543916.1:c.1670G>A	XP_011542218.1:p.Cys557Tyr
XM_011543917.1:c.1289G>A	XP_011542219.1:p.Cys430Tyr
XM_011543918.1:c.1526G>A	XP_011542220.1:p.Cys509Tyr
XM_011543919.1:c.1490G>A	XP_011542221.1:p.Cys497Tyr
XM_017029567.1:c.1397G>A	XP_016885056.1:p.Cys466Tyr