Canonical Allele Identifier: CA412951099

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49112197C>T (hg19) ; chrX:g.49255736C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255736C>T , CM000685.2:g.49255736C>T	GRCh38
NC_000023.10:g.49112197C>T , CM000685.1:g.49112197C>T	GRCh37
NC_000023.9:g.48999141C>T	NCBI36
NG_007392.1:g.14092G>A , LRG_62:g.14092G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.609G>A	ENSP00000365372.2:p.Met203Ile
ENST00000376207.10:c.714G>A MANE Select	ENSP00000365380.4:p.Met238Ile
ENST00000455775.7:c.783G>A	ENSP00000396415.3:p.Met261Ile
ENST00000518685.6:c.714G>A	ENSP00000428952.2:p.Met238Ile
ENST00000557224.6:c.609G>A	ENSP00000451208.1:p.Met203Ile
ENST00000651307.1:c.714G>A	ENSP00000498454.1:p.Met238Ile
ENST00000376197.1:c.564G>A	ENSP00000365369.1:p.Met188Ile
ENST00000376199.6:c.609G>A	ENSP00000365372.2:p.Met203Ile
ENST00000376207.8:c.714G>A	ENSP00000365380.4:p.Met238Ile
ENST00000455775.6:c.783G>A	ENSP00000396415.3:p.Met261Ile
ENST00000518685.5:c.609G>A	ENSP00000428952.1:p.Met203Ile
ENST00000557224.5:c.609G>A	ENSP00000451208.1:p.Met203Ile
NM_001114377.1:c.609G>A	NP_001107849.1:p.Met203Ile
NM_014009.3:c.714G>A , LRG_62t1:c.714G>A	NP_054728.2:p.Met238Ile
XM_006724533.2:c.783G>A	XP_006724596.2:p.Met261Ile
XM_011543915.1:c.933G>A	XP_011542217.1:p.Met311Ile
XM_011543916.1:c.933G>A	XP_011542218.1:p.Met311Ile
XM_011543917.1:c.732G>A	XP_011542219.1:p.Met244Ile
XM_011543918.1:c.969G>A	XP_011542220.1:p.Met323Ile
XM_011543919.1:c.933G>A	XP_011542221.1:p.Met311Ile
XM_017029567.1:c.660G>A	XP_016885056.1:p.Met220Ile
NM_001114377.2:c.609G>A	NP_001107849.1:p.Met203Ile
NM_014009.4:c.714G>A MANE Select	NP_054728.2:p.Met238Ile