Canonical Allele Identifier: CA412948741

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108153A>G (hg19) ; chrX:g.49251692A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251692A>G , CM000685.2:g.49251692A>G	GRCh38
NC_000023.10:g.49108153A>G , CM000685.1:g.49108153A>G	GRCh37
NC_000023.9:g.48995097A>G	NCBI36
NG_007392.1:g.18136T>C , LRG_62:g.18136T>C
NG_021311.2:g.21228A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.1013T>C	ENSP00000365372.2:p.Phe338Ser
ENST00000376207.10:c.1118T>C MANE Select	ENSP00000365380.4:p.Phe373Ser
ENST00000455775.7:c.1187T>C	ENSP00000396415.3:p.Phe396Ser
ENST00000518685.6:c.1037T>C	ENSP00000428952.2:p.Phe346Ser
ENST00000557224.6:c.1013T>C	ENSP00000451208.1:p.Phe338Ser
ENST00000651307.1:c.*33T>C	ENSP00000498454.1:n.*33T>C
ENST00000376197.1:c.968T>C	ENSP00000365369.1:p.Phe323Ser
ENST00000376199.6:c.1013T>C	ENSP00000365372.2:p.Phe338Ser
ENST00000376207.8:c.1118T>C	ENSP00000365380.4:p.Phe373Ser
ENST00000455775.6:c.1187T>C	ENSP00000396415.3:p.Phe396Ser
ENST00000518685.5:c.1013T>C	ENSP00000428952.1:p.Phe338Ser
ENST00000557224.5:c.1013T>C	ENSP00000451208.1:p.Phe338Ser
NM_001114377.1:c.1013T>C	NP_001107849.1:p.Phe338Ser
NM_014009.3:c.1118T>C , LRG_62t1:c.1118T>C	NP_054728.2:p.Phe373Ser
XM_006724533.2:c.1187T>C	XP_006724596.2:p.Phe396Ser
XM_011543915.1:c.1337T>C	XP_011542217.1:p.Phe446Ser
XM_011543916.1:c.1337T>C	XP_011542218.1:p.Phe446Ser
XM_011543917.1:c.1136T>C	XP_011542219.1:p.Phe379Ser
XM_011543918.1:c.1373T>C	XP_011542220.1:p.Phe458Ser
XM_011543919.1:c.1337T>C	XP_011542221.1:p.Phe446Ser
XM_017029567.1:c.1064T>C	XP_016885056.1:p.Phe355Ser
NM_001114377.2:c.1013T>C	NP_001107849.1:p.Phe338Ser
NM_014009.4:c.1118T>C MANE Select	NP_054728.2:p.Phe373Ser