Canonical Allele Identifier: CA329136702

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49257026C>T , CM000685.2:g.49257026C>T	GRCh38
NC_000023.10:g.49113483C>T , CM000685.1:g.49113483C>T	GRCh37
NC_000023.9:g.49000427C>T	NCBI36
NG_007392.1:g.12806G>A , LRG_62:g.12806G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014009.4:c.455-14G>A MANE Select	NP_054728.2:n.455-14G>A
ENST00000376207.10:c.455-14G>A MANE Select	ENSP00000365380.4:n.455-14G>A
NM_001114377.1:c.350-14G>A	NP_001107849.1:n.350-14G>A
NM_001114377.2:c.350-14G>A	NP_001107849.1:n.350-14G>A
NM_014009.3:c.455-14G>A , LRG_62t1:c.455-14G>A	NP_054728.2:n.455-14G>A
ENST00000376197.1:c.305-14G>A	ENSP00000365369.1:n.305-14G>A
ENST00000376199.6:c.350-14G>A	ENSP00000365372.2:n.350-14G>A
ENST00000376199.7:c.350-14G>A	ENSP00000365372.2:n.350-14G>A
ENST00000376207.8:c.455-14G>A	ENSP00000365380.4:n.455-14G>A
ENST00000455775.6:c.455-14G>A	ENSP00000396415.3:n.455-14G>A
ENST00000455775.7:c.455-14G>A	ENSP00000396415.3:n.455-14G>A
ENST00000518685.5:c.350-14G>A	ENSP00000428952.1:n.350-14G>A
ENST00000518685.6:c.455-14G>A	ENSP00000428952.2:n.455-14G>A
ENST00000557224.5:c.350-14G>A	ENSP00000451208.1:n.350-14G>A
ENST00000557224.6:c.350-14G>A	ENSP00000451208.1:n.350-14G>A
ENST00000651307.1:c.455-14G>A	ENSP00000498454.1:n.455-14G>A
ENST00000652559.1:c.308-14G>A	ENSP00000498236.1:n.308-14G>A
XM_006724533.2:c.455-14G>A	XP_006724596.2:n.455-14G>A
XM_011543915.1:c.674-14G>A	XP_011542217.1:n.674-14G>A
XM_011543916.1:c.674-14G>A	XP_011542218.1:n.674-14G>A
XM_011543917.1:c.473-14G>A	XP_011542219.1:n.473-14G>A
XM_011543918.1:c.710-14G>A	XP_011542220.1:n.710-14G>A
XM_011543919.1:c.674-14G>A	XP_011542221.1:n.674-14G>A
XM_017029567.1:c.401-14G>A	XP_016885056.1:n.401-14G>A