Canonical Allele Identifier: CA10411770

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49256767G>C , CM000685.2:g.49256767G>C	GRCh38
NC_000023.10:g.49113224G>C , CM000685.1:g.49113224G>C	GRCh37
NC_000023.9:g.49000168G>C	NCBI36
NG_007392.1:g.13065C>G , LRG_62:g.13065C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_014009.4:c.631C>G MANE Select	NP_054728.2:p.Pro211Ala
ENST00000376207.10:c.631C>G MANE Select	ENSP00000365380.4:p.Pro211Ala
NM_001114377.1:c.526C>G	NP_001107849.1:p.Pro176Ala
NM_001114377.2:c.526C>G	NP_001107849.1:p.Pro176Ala
NM_014009.3:c.631C>G , LRG_62t1:c.631C>G	NP_054728.2:p.Pro211Ala
ENST00000376197.1:c.481C>G	ENSP00000365369.1:p.Pro161Ala
ENST00000376199.6:c.526C>G	ENSP00000365372.2:p.Pro176Ala
ENST00000376199.7:c.526C>G	ENSP00000365372.2:p.Pro176Ala
ENST00000376207.8:c.631C>G	ENSP00000365380.4:p.Pro211Ala
ENST00000455775.6:c.700C>G	ENSP00000396415.3:p.Pro234Ala
ENST00000455775.7:c.700C>G	ENSP00000396415.3:p.Pro234Ala
ENST00000518685.5:c.526C>G	ENSP00000428952.1:p.Pro176Ala
ENST00000518685.6:c.631C>G	ENSP00000428952.2:p.Pro211Ala
ENST00000557224.5:c.526C>G	ENSP00000451208.1:p.Pro176Ala
ENST00000557224.6:c.526C>G	ENSP00000451208.1:p.Pro176Ala
ENST00000651307.1:c.631C>G	ENSP00000498454.1:p.Pro211Ala
XM_006724533.2:c.700C>G	XP_006724596.2:p.Pro234Ala
XM_011543915.1:c.850C>G	XP_011542217.1:p.Pro284Ala
XM_011543916.1:c.850C>G	XP_011542218.1:p.Pro284Ala
XM_011543917.1:c.649C>G	XP_011542219.1:p.Pro217Ala
XM_011543918.1:c.886C>G	XP_011542220.1:p.Pro296Ala
XM_011543919.1:c.850C>G	XP_011542221.1:p.Pro284Ala
XM_017029567.1:c.577C>G	XP_016885056.1:p.Pro193Ala