Canonical Allele Identifier: CA412950264

Gene: FOXP3

Linked Data

• gnomAD v4: X-49253170-G-T
• MyVariant Identifiers: chrX:g.49109631G>T (hg19) ; chrX:g.49253170G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49253170G>T , CM000685.2:g.49253170G>T	GRCh38
NC_000023.10:g.49109631G>T , CM000685.1:g.49109631G>T	GRCh37
NC_000023.9:g.48996575G>T	NCBI36
NG_007392.1:g.16658C>A , LRG_62:g.16658C>A
NG_021311.2:g.22706G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.895C>A	ENSP00000365372.2:p.His299Asn
ENST00000376207.10:c.1000C>A MANE Select	ENSP00000365380.4:p.His334Asn
ENST00000455775.7:c.1069C>A	ENSP00000396415.3:p.His357Asn
ENST00000518685.6:c.919C>A	ENSP00000428952.2:p.His307Asn
ENST00000557224.6:c.895C>A	ENSP00000451208.1:p.His299Asn
ENST00000651307.1:c.967+747C>A	ENSP00000498454.1:n.967+747C>A
ENST00000376197.1:c.850C>A	ENSP00000365369.1:p.His284Asn
ENST00000376199.6:c.895C>A	ENSP00000365372.2:p.His299Asn
ENST00000376207.8:c.1000C>A	ENSP00000365380.4:p.His334Asn
ENST00000455775.6:c.1069C>A	ENSP00000396415.3:p.His357Asn
ENST00000518685.5:c.895C>A	ENSP00000428952.1:p.His299Asn
ENST00000557224.5:c.895C>A	ENSP00000451208.1:p.His299Asn
NM_001114377.1:c.895C>A	NP_001107849.1:p.His299Asn
NM_014009.3:c.1000C>A , LRG_62t1:c.1000C>A	NP_054728.2:p.His334Asn
XM_006724533.2:c.1069C>A	XP_006724596.2:p.His357Asn
XM_011543915.1:c.1219C>A	XP_011542217.1:p.His407Asn
XM_011543916.1:c.1219C>A	XP_011542218.1:p.His407Asn
XM_011543917.1:c.1018C>A	XP_011542219.1:p.His340Asn
XM_011543918.1:c.1255C>A	XP_011542220.1:p.His419Asn
XM_011543919.1:c.1219C>A	XP_011542221.1:p.His407Asn
XM_017029567.1:c.946C>A	XP_016885056.1:p.His316Asn
NM_001114377.2:c.895C>A	NP_001107849.1:p.His299Asn
NM_014009.4:c.1000C>A MANE Select	NP_054728.2:p.His334Asn