Canonical Allele Identifier: CA516397021

Gene: FOXP3

Linked Data

• gnomAD v4: X-49255438-A-G
• MyVariant Identifiers: chrX:g.49111899A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255438A>G , CM000685.2:g.49255438A>G	GRCh38
NC_000023.10:g.49111899A>G , CM000685.1:g.49111899A>G	GRCh37
NC_000023.9:g.48998843A>G	NCBI36
NG_007392.1:g.14390T>C , LRG_62:g.14390T>C
NG_021311.2:g.24974A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.702T>C	ENSP00000365372.2:p.Ala234=
ENST00000376207.10:c.807T>C MANE Select	ENSP00000365380.4:p.Ala269=
ENST00000455775.7:c.876T>C	ENSP00000396415.3:p.Ala292=
ENST00000518685.6:c.735+277T>C	ENSP00000428952.2:n.735+277T>C
ENST00000557224.6:c.702T>C	ENSP00000451208.1:p.Ala234=
ENST00000651307.1:c.807T>C	ENSP00000498454.1:p.Ala269=
ENST00000376197.1:c.657T>C	ENSP00000365369.1:p.Ala219=
ENST00000376199.6:c.702T>C	ENSP00000365372.2:p.Ala234=
ENST00000376207.8:c.807T>C	ENSP00000365380.4:p.Ala269=
ENST00000455775.6:c.876T>C	ENSP00000396415.3:p.Ala292=
ENST00000518685.5:c.702T>C	ENSP00000428952.1:p.Ala234=
ENST00000557224.5:c.702T>C	ENSP00000451208.1:p.Ala234=
NM_001114377.1:c.702T>C	NP_001107849.1:p.Ala234=
NM_014009.3:c.807T>C , LRG_62t1:c.807T>C	NP_054728.2:p.Ala269=
XM_006724533.2:c.876T>C	XP_006724596.2:p.Ala292=
XM_011543915.1:c.1026T>C	XP_011542217.1:p.Ala342=
XM_011543916.1:c.1026T>C	XP_011542218.1:p.Ala342=
XM_011543917.1:c.825T>C	XP_011542219.1:p.Ala275=
XM_011543918.1:c.1062T>C	XP_011542220.1:p.Ala354=
XM_011543919.1:c.1026T>C	XP_011542221.1:p.Ala342=
XM_017029567.1:c.753T>C	XP_016885056.1:p.Ala251=
NM_001114377.2:c.702T>C	NP_001107849.1:p.Ala234=
NM_014009.4:c.807T>C MANE Select	NP_054728.2:p.Ala269=