Canonical Allele Identifier: CA412950964

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49111939A>G (hg19) ; chrX:g.49255478A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255478A>G , CM000685.2:g.49255478A>G	GRCh38
NC_000023.10:g.49111939A>G , CM000685.1:g.49111939A>G	GRCh37
NC_000023.9:g.48998883A>G	NCBI36
NG_007392.1:g.14350T>C , LRG_62:g.14350T>C
NG_021311.2:g.25014A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.662T>C	ENSP00000365372.2:p.Met221Thr
ENST00000376207.10:c.767T>C MANE Select	ENSP00000365380.4:p.Met256Thr
ENST00000455775.7:c.836T>C	ENSP00000396415.3:p.Met279Thr
ENST00000518685.6:c.735+237T>C	ENSP00000428952.2:n.735+237T>C
ENST00000557224.6:c.662T>C	ENSP00000451208.1:p.Met221Thr
ENST00000651307.1:c.767T>C	ENSP00000498454.1:p.Met256Thr
ENST00000376197.1:c.617T>C	ENSP00000365369.1:p.Met206Thr
ENST00000376199.6:c.662T>C	ENSP00000365372.2:p.Met221Thr
ENST00000376207.8:c.767T>C	ENSP00000365380.4:p.Met256Thr
ENST00000455775.6:c.836T>C	ENSP00000396415.3:p.Met279Thr
ENST00000518685.5:c.662T>C	ENSP00000428952.1:p.Met221Thr
ENST00000557224.5:c.662T>C	ENSP00000451208.1:p.Met221Thr
NM_001114377.1:c.662T>C	NP_001107849.1:p.Met221Thr
NM_014009.3:c.767T>C , LRG_62t1:c.767T>C	NP_054728.2:p.Met256Thr
XM_006724533.2:c.836T>C	XP_006724596.2:p.Met279Thr
XM_011543915.1:c.986T>C	XP_011542217.1:p.Met329Thr
XM_011543916.1:c.986T>C	XP_011542218.1:p.Met329Thr
XM_011543917.1:c.785T>C	XP_011542219.1:p.Met262Thr
XM_011543918.1:c.1022T>C	XP_011542220.1:p.Met341Thr
XM_011543919.1:c.986T>C	XP_011542221.1:p.Met329Thr
XM_017029567.1:c.713T>C	XP_016885056.1:p.Met238Thr
NM_001114377.2:c.662T>C	NP_001107849.1:p.Met221Thr
NM_014009.4:c.767T>C MANE Select	NP_054728.2:p.Met256Thr