Canonical Allele Identifier: CA412949001

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108214C>G (hg19) ; chrX:g.49251753C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251753C>G , CM000685.2:g.49251753C>G	GRCh38
NC_000023.10:g.49108214C>G , CM000685.1:g.49108214C>G	GRCh37
NC_000023.9:g.48995158C>G	NCBI36
NG_007392.1:g.18075G>C , LRG_62:g.18075G>C
NG_021311.2:g.21289C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.952G>C	ENSP00000365372.2:p.Ala318Pro
ENST00000376207.10:c.1057G>C MANE Select	ENSP00000365380.4:p.Ala353Pro
ENST00000455775.7:c.1126G>C	ENSP00000396415.3:p.Ala376Pro
ENST00000518685.6:c.976G>C	ENSP00000428952.2:p.Ala326Pro
ENST00000557224.6:c.952G>C	ENSP00000451208.1:p.Ala318Pro
ENST00000651307.1:c.980G>C	ENSP00000498454.1:p.Gly327Ala
ENST00000376197.1:c.907G>C	ENSP00000365369.1:p.Ala303Pro
ENST00000376199.6:c.952G>C	ENSP00000365372.2:p.Ala318Pro
ENST00000376207.8:c.1057G>C	ENSP00000365380.4:p.Ala353Pro
ENST00000455775.6:c.1126G>C	ENSP00000396415.3:p.Ala376Pro
ENST00000518685.5:c.952G>C	ENSP00000428952.1:p.Ala318Pro
ENST00000557224.5:c.952G>C	ENSP00000451208.1:p.Ala318Pro
NM_001114377.1:c.952G>C	NP_001107849.1:p.Ala318Pro
NM_014009.3:c.1057G>C , LRG_62t1:c.1057G>C	NP_054728.2:p.Ala353Pro
XM_006724533.2:c.1126G>C	XP_006724596.2:p.Ala376Pro
XM_011543915.1:c.1276G>C	XP_011542217.1:p.Ala426Pro
XM_011543916.1:c.1276G>C	XP_011542218.1:p.Ala426Pro
XM_011543917.1:c.1075G>C	XP_011542219.1:p.Ala359Pro
XM_011543918.1:c.1312G>C	XP_011542220.1:p.Ala438Pro
XM_011543919.1:c.1276G>C	XP_011542221.1:p.Ala426Pro
XM_017029567.1:c.1003G>C	XP_016885056.1:p.Ala335Pro
NM_001114377.2:c.952G>C	NP_001107849.1:p.Ala318Pro
NM_014009.4:c.1057G>C MANE Select	NP_054728.2:p.Ala353Pro