Canonical Allele Identifier: CA516397227

Gene: FOXP3

Linked Data

• COSMIC: COSM5965576
• MyVariant Identifiers: chrX:g.49111965C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255504C>G , CM000685.2:g.49255504C>G	GRCh38
NC_000023.10:g.49111965C>G , CM000685.1:g.49111965C>G	GRCh37
NC_000023.9:g.48998909C>G	NCBI36
NG_007392.1:g.14324G>C , LRG_62:g.14324G>C
NG_021311.2:g.25040C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.636G>C	ENSP00000365372.2:p.Val212=
ENST00000376207.10:c.741G>C MANE Select	ENSP00000365380.4:p.Val247=
ENST00000455775.7:c.810G>C	ENSP00000396415.3:p.Val270=
ENST00000518685.6:c.735+211G>C	ENSP00000428952.2:n.735+211G>C
ENST00000557224.6:c.636G>C	ENSP00000451208.1:p.Val212=
ENST00000651307.1:c.741G>C	ENSP00000498454.1:p.Val247=
ENST00000376197.1:c.591G>C	ENSP00000365369.1:p.Val197=
ENST00000376199.6:c.636G>C	ENSP00000365372.2:p.Val212=
ENST00000376207.8:c.741G>C	ENSP00000365380.4:p.Val247=
ENST00000455775.6:c.810G>C	ENSP00000396415.3:p.Val270=
ENST00000518685.5:c.636G>C	ENSP00000428952.1:p.Val212=
ENST00000557224.5:c.636G>C	ENSP00000451208.1:p.Val212=
NM_001114377.1:c.636G>C	NP_001107849.1:p.Val212=
NM_014009.3:c.741G>C , LRG_62t1:c.741G>C	NP_054728.2:p.Val247=
XM_006724533.2:c.810G>C	XP_006724596.2:p.Val270=
XM_011543915.1:c.960G>C	XP_011542217.1:p.Val320=
XM_011543916.1:c.960G>C	XP_011542218.1:p.Val320=
XM_011543917.1:c.759G>C	XP_011542219.1:p.Val253=
XM_011543918.1:c.996G>C	XP_011542220.1:p.Val332=
XM_011543919.1:c.960G>C	XP_011542221.1:p.Val320=
XM_017029567.1:c.687G>C	XP_016885056.1:p.Val229=
NM_001114377.2:c.636G>C	NP_001107849.1:p.Val212=
NM_014009.4:c.741G>C MANE Select	NP_054728.2:p.Val247=