Canonical Allele Identifier: CA10411807

Gene: FOXP3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49257447G>T , CM000685.2:g.49257447G>T	GRCh38
NC_000023.10:g.49113904G>T , CM000685.1:g.49113904G>T	GRCh37
NC_000023.9:g.49000848G>T	NCBI36
NG_007392.1:g.12385C>A , LRG_62:g.12385C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.329C>A	ENSP00000365372.2:p.Ala110Asp
ENST00000376207.10:c.434C>A MANE Select	ENSP00000365380.4:p.Ala145Asp
ENST00000455775.7:c.434C>A	ENSP00000396415.3:p.Ala145Asp
ENST00000518685.6:c.434C>A	ENSP00000428952.2:p.Ala145Asp
ENST00000557224.6:c.329C>A	ENSP00000451208.1:p.Ala110Asp
ENST00000651307.1:c.434C>A	ENSP00000498454.1:p.Ala145Asp
ENST00000652559.1:c.287C>A	ENSP00000498236.1:p.Ala96Asp
ENST00000376197.1:c.284C>A	ENSP00000365369.1:p.Ala95Asp
ENST00000376199.6:c.329C>A	ENSP00000365372.2:p.Ala110Asp
ENST00000376207.8:c.434C>A	ENSP00000365380.4:p.Ala145Asp
ENST00000455775.6:c.434C>A	ENSP00000396415.3:p.Ala145Asp
ENST00000518685.5:c.329C>A	ENSP00000428952.1:p.Ala110Asp
ENST00000557224.5:c.329C>A	ENSP00000451208.1:p.Ala110Asp
NM_001114377.1:c.329C>A	NP_001107849.1:p.Ala110Asp
NM_014009.3:c.434C>A , LRG_62t1:c.434C>A	NP_054728.2:p.Ala145Asp
XM_006724533.2:c.434C>A	XP_006724596.2:p.Ala145Asp
XM_011543915.1:c.653C>A	XP_011542217.1:p.Ala218Asp
XM_011543916.1:c.653C>A	XP_011542218.1:p.Ala218Asp
XM_011543917.1:c.452C>A	XP_011542219.1:p.Ala151Asp
XM_011543918.1:c.689C>A	XP_011542220.1:p.Ala230Asp
XM_011543919.1:c.653C>A	XP_011542221.1:p.Ala218Asp
XM_017029567.1:c.380C>A	XP_016885056.1:p.Ala127Asp
NM_001114377.2:c.329C>A	NP_001107849.1:p.Ala110Asp
NM_014009.4:c.434C>A MANE Select	NP_054728.2:p.Ala145Asp