Canonical Allele Identifier: CA516396996

Gene: FOXP3

Linked Data

• gnomAD v4: X-49255429-C-A
• MyVariant Identifiers: chrX:g.49111890C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255429C>A , CM000685.2:g.49255429C>A	GRCh38
NC_000023.10:g.49111890C>A , CM000685.1:g.49111890C>A	GRCh37
NC_000023.9:g.48998834C>A	NCBI36
NG_007392.1:g.14399G>T , LRG_62:g.14399G>T
NG_021311.2:g.24965C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.711G>T	ENSP00000365372.2:p.Val237=
ENST00000376207.10:c.816G>T MANE Select	ENSP00000365380.4:p.Val272=
ENST00000455775.7:c.885G>T	ENSP00000396415.3:p.Val295=
ENST00000518685.6:c.735+286G>T	ENSP00000428952.2:n.735+286G>T
ENST00000557224.6:c.711G>T	ENSP00000451208.1:p.Val237=
ENST00000651307.1:c.816G>T	ENSP00000498454.1:p.Val272=
ENST00000376197.1:c.666G>T	ENSP00000365369.1:p.Val222=
ENST00000376199.6:c.711G>T	ENSP00000365372.2:p.Val237=
ENST00000376207.8:c.816G>T	ENSP00000365380.4:p.Val272=
ENST00000455775.6:c.885G>T	ENSP00000396415.3:p.Val295=
ENST00000518685.5:c.711G>T	ENSP00000428952.1:p.Val237=
ENST00000557224.5:c.711G>T	ENSP00000451208.1:p.Val237=
NM_001114377.1:c.711G>T	NP_001107849.1:p.Val237=
NM_014009.3:c.816G>T , LRG_62t1:c.816G>T	NP_054728.2:p.Val272=
XM_006724533.2:c.885G>T	XP_006724596.2:p.Val295=
XM_011543915.1:c.1035G>T	XP_011542217.1:p.Val345=
XM_011543916.1:c.1035G>T	XP_011542218.1:p.Val345=
XM_011543917.1:c.834G>T	XP_011542219.1:p.Val278=
XM_011543918.1:c.1071G>T	XP_011542220.1:p.Val357=
XM_011543919.1:c.1035G>T	XP_011542221.1:p.Val345=
XM_017029567.1:c.762G>T	XP_016885056.1:p.Val254=
NM_001114377.2:c.711G>T	NP_001107849.1:p.Val237=
NM_014009.4:c.816G>T MANE Select	NP_054728.2:p.Val272=