Canonical Allele Identifier: CA412950927

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49111924G>A (hg19) ; chrX:g.49255463G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255463G>A , CM000685.2:g.49255463G>A	GRCh38
NC_000023.10:g.49111924G>A , CM000685.1:g.49111924G>A	GRCh37
NC_000023.9:g.48998868G>A	NCBI36
NG_007392.1:g.14365C>T , LRG_62:g.14365C>T
NG_021311.2:g.24999G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.677C>T	ENSP00000365372.2:p.Ala226Val
ENST00000376207.10:c.782C>T MANE Select	ENSP00000365380.4:p.Ala261Val
ENST00000455775.7:c.851C>T	ENSP00000396415.3:p.Ala284Val
ENST00000518685.6:c.735+252C>T	ENSP00000428952.2:n.735+252C>T
ENST00000557224.6:c.677C>T	ENSP00000451208.1:p.Ala226Val
ENST00000651307.1:c.782C>T	ENSP00000498454.1:p.Ala261Val
ENST00000376197.1:c.632C>T	ENSP00000365369.1:p.Ala211Val
ENST00000376199.6:c.677C>T	ENSP00000365372.2:p.Ala226Val
ENST00000376207.8:c.782C>T	ENSP00000365380.4:p.Ala261Val
ENST00000455775.6:c.851C>T	ENSP00000396415.3:p.Ala284Val
ENST00000518685.5:c.677C>T	ENSP00000428952.1:p.Ala226Val
ENST00000557224.5:c.677C>T	ENSP00000451208.1:p.Ala226Val
NM_001114377.1:c.677C>T	NP_001107849.1:p.Ala226Val
NM_014009.3:c.782C>T , LRG_62t1:c.782C>T	NP_054728.2:p.Ala261Val
XM_006724533.2:c.851C>T	XP_006724596.2:p.Ala284Val
XM_011543915.1:c.1001C>T	XP_011542217.1:p.Ala334Val
XM_011543916.1:c.1001C>T	XP_011542218.1:p.Ala334Val
XM_011543917.1:c.800C>T	XP_011542219.1:p.Ala267Val
XM_011543918.1:c.1037C>T	XP_011542220.1:p.Ala346Val
XM_011543919.1:c.1001C>T	XP_011542221.1:p.Ala334Val
XM_017029567.1:c.728C>T	XP_016885056.1:p.Ala243Val
NM_001114377.2:c.677C>T	NP_001107849.1:p.Ala226Val
NM_014009.4:c.782C>T MANE Select	NP_054728.2:p.Ala261Val