Canonical Allele Identifier: CA412948961

Gene: FOXP3

Linked Data

• gnomAD v4: X-49251739-C-A
• MyVariant Identifiers: chrX:g.49108200C>A (hg19) ; chrX:g.49251739C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251739C>A , CM000685.2:g.49251739C>A	GRCh38
NC_000023.10:g.49108200C>A , CM000685.1:g.49108200C>A	GRCh37
NC_000023.9:g.48995144C>A	NCBI36
NG_007392.1:g.18089G>T , LRG_62:g.18089G>T
NG_021311.2:g.21275C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.966G>T	ENSP00000365372.2:p.Gln322His
ENST00000376207.10:c.1071G>T MANE Select	ENSP00000365380.4:p.Gln357His
ENST00000455775.7:c.1140G>T	ENSP00000396415.3:p.Gln380His
ENST00000518685.6:c.990G>T	ENSP00000428952.2:p.Gln330His
ENST00000557224.6:c.966G>T	ENSP00000451208.1:p.Gln322His
ENST00000651307.1:c.994G>T	ENSP00000498454.1:p.Ala332Ser
ENST00000376197.1:c.921G>T	ENSP00000365369.1:p.Gln307His
ENST00000376199.6:c.966G>T	ENSP00000365372.2:p.Gln322His
ENST00000376207.8:c.1071G>T	ENSP00000365380.4:p.Gln357His
ENST00000455775.6:c.1140G>T	ENSP00000396415.3:p.Gln380His
ENST00000518685.5:c.966G>T	ENSP00000428952.1:p.Gln322His
ENST00000557224.5:c.966G>T	ENSP00000451208.1:p.Gln322His
NM_001114377.1:c.966G>T	NP_001107849.1:p.Gln322His
NM_014009.3:c.1071G>T , LRG_62t1:c.1071G>T	NP_054728.2:p.Gln357His
XM_006724533.2:c.1140G>T	XP_006724596.2:p.Gln380His
XM_011543915.1:c.1290G>T	XP_011542217.1:p.Gln430His
XM_011543916.1:c.1290G>T	XP_011542218.1:p.Gln430His
XM_011543917.1:c.1089G>T	XP_011542219.1:p.Gln363His
XM_011543918.1:c.1326G>T	XP_011542220.1:p.Gln442His
XM_011543919.1:c.1290G>T	XP_011542221.1:p.Gln430His
XM_017029567.1:c.1017G>T	XP_016885056.1:p.Gln339His
NM_001114377.2:c.966G>T	NP_001107849.1:p.Gln322His
NM_014009.4:c.1071G>T MANE Select	NP_054728.2:p.Gln357His