Canonical Allele Identifier: CA875963348

Gene: FOXP3

Linked Data

• dbSNP Id: rs1178314364
• gnomAD v3: X-49261735-C-T
• gnomAD v4: X-49261735-C-T
• MyVariant Identifiers: chrX:g.49261735C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49261735C>T , CM000685.2:g.49261735C>T	GRCh38
NC_000023.10:g.49118192C>T , CM000685.1:g.49118192C>T	GRCh37
NC_000023.9:g.49005136C>T	NCBI36
NG_007392.1:g.8097G>A , LRG_62:g.8097G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000703450.1:c.-22-3208G>A	ENSP00000515301.1:n.-22-3208G>A
ENST00000684155.1:c.-23+2926G>A	ENSP00000507726.1:n.-23+2926G>A
ENST00000376199.7:c.-23+2926G>A	ENSP00000365372.2:n.-23+2926G>A
ENST00000376207.10:c.-23+2926G>A MANE Select	ENSP00000365380.4:n.-23+2926G>A
ENST00000455775.7:c.-23+2926G>A	ENSP00000396415.3:n.-23+2926G>A
ENST00000557224.6:c.-23+2926G>A	ENSP00000451208.1:n.-23+2926G>A
ENST00000650877.1:c.-22-3208G>A	ENSP00000499100.1:n.-22-3208G>A
ENST00000652559.1:c.-23+2926G>A	ENSP00000498236.1:n.-23+2926G>A
ENST00000376199.6:c.-23+2926G>A	ENSP00000365372.2:n.-23+2926G>A
ENST00000376207.8:c.-23+2926G>A	ENSP00000365380.4:n.-23+2926G>A
ENST00000455775.6:c.-23+2926G>A	ENSP00000396415.3:n.-23+2926G>A
NM_001114377.1:c.-23+2926G>A	NP_001107849.1:n.-23+2926G>A
NM_014009.3:c.-23+2926G>A , LRG_62t1:c.-23+2926G>A	NP_054728.2:n.-23+2926G>A
XM_006724533.2:c.-23+2926G>A	XP_006724596.2:n.-23+2926G>A
XM_011543915.1:c.302+2926G>A	XP_011542217.1:n.302+2926G>A
XM_011543916.1:c.302+2926G>A	XP_011542218.1:n.302+2926G>A
XM_011543917.1:c.-23+2926G>A	XP_011542219.1:n.-23+2926G>A
XM_011543918.1:c.302+2926G>A	XP_011542220.1:n.302+2926G>A
XM_011543919.1:c.302+2926G>A	XP_011542221.1:n.302+2926G>A
XM_017029567.1:c.29+2796G>A	XP_016885056.1:n.29+2796G>A
NM_001114377.2:c.-23+2926G>A	NP_001107849.1:n.-23+2926G>A
NM_014009.4:c.-23+2926G>A MANE Select	NP_054728.2:n.-23+2926G>A