Canonical Allele Identifier: CA412951101

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49112198A>G (hg19) ; chrX:g.49255737A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255737A>G , CM000685.2:g.49255737A>G	GRCh38
NC_000023.10:g.49112198A>G , CM000685.1:g.49112198A>G	GRCh37
NC_000023.9:g.48999142A>G	NCBI36
NG_007392.1:g.14091T>C , LRG_62:g.14091T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.608T>C	ENSP00000365372.2:p.Met203Thr
ENST00000376207.10:c.713T>C MANE Select	ENSP00000365380.4:p.Met238Thr
ENST00000455775.7:c.782T>C	ENSP00000396415.3:p.Met261Thr
ENST00000518685.6:c.713T>C	ENSP00000428952.2:p.Met238Thr
ENST00000557224.6:c.608T>C	ENSP00000451208.1:p.Met203Thr
ENST00000651307.1:c.713T>C	ENSP00000498454.1:p.Met238Thr
ENST00000376197.1:c.563T>C	ENSP00000365369.1:p.Met188Thr
ENST00000376199.6:c.608T>C	ENSP00000365372.2:p.Met203Thr
ENST00000376207.8:c.713T>C	ENSP00000365380.4:p.Met238Thr
ENST00000455775.6:c.782T>C	ENSP00000396415.3:p.Met261Thr
ENST00000518685.5:c.608T>C	ENSP00000428952.1:p.Met203Thr
ENST00000557224.5:c.608T>C	ENSP00000451208.1:p.Met203Thr
NM_001114377.1:c.608T>C	NP_001107849.1:p.Met203Thr
NM_014009.3:c.713T>C , LRG_62t1:c.713T>C	NP_054728.2:p.Met238Thr
XM_006724533.2:c.782T>C	XP_006724596.2:p.Met261Thr
XM_011543915.1:c.932T>C	XP_011542217.1:p.Met311Thr
XM_011543916.1:c.932T>C	XP_011542218.1:p.Met311Thr
XM_011543917.1:c.731T>C	XP_011542219.1:p.Met244Thr
XM_011543918.1:c.968T>C	XP_011542220.1:p.Met323Thr
XM_011543919.1:c.932T>C	XP_011542221.1:p.Met311Thr
XM_017029567.1:c.659T>C	XP_016885056.1:p.Met220Thr
NM_001114377.2:c.608T>C	NP_001107849.1:p.Met203Thr
NM_014009.4:c.713T>C MANE Select	NP_054728.2:p.Met238Thr