Canonical Allele Identifier: CA412948781

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108162A>C (hg19) ; chrX:g.49251701A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251701A>C , CM000685.2:g.49251701A>C	GRCh38
NC_000023.10:g.49108162A>C , CM000685.1:g.49108162A>C	GRCh37
NC_000023.9:g.48995106A>C	NCBI36
NG_007392.1:g.18127T>G , LRG_62:g.18127T>G
NG_021311.2:g.21237A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.1004T>G	ENSP00000365372.2:p.Met335Arg
ENST00000376207.10:c.1109T>G MANE Select	ENSP00000365380.4:p.Met370Arg
ENST00000455775.7:c.1178T>G	ENSP00000396415.3:p.Met393Arg
ENST00000518685.6:c.1028T>G	ENSP00000428952.2:p.Met343Arg
ENST00000557224.6:c.1004T>G	ENSP00000451208.1:p.Met335Arg
ENST00000651307.1:c.*24T>G	ENSP00000498454.1:n.*24T>G
ENST00000376197.1:c.959T>G	ENSP00000365369.1:p.Met320Arg
ENST00000376199.6:c.1004T>G	ENSP00000365372.2:p.Met335Arg
ENST00000376207.8:c.1109T>G	ENSP00000365380.4:p.Met370Arg
ENST00000455775.6:c.1178T>G	ENSP00000396415.3:p.Met393Arg
ENST00000518685.5:c.1004T>G	ENSP00000428952.1:p.Met335Arg
ENST00000557224.5:c.1004T>G	ENSP00000451208.1:p.Met335Arg
NM_001114377.1:c.1004T>G	NP_001107849.1:p.Met335Arg
NM_014009.3:c.1109T>G , LRG_62t1:c.1109T>G	NP_054728.2:p.Met370Arg
XM_006724533.2:c.1178T>G	XP_006724596.2:p.Met393Arg
XM_011543915.1:c.1328T>G	XP_011542217.1:p.Met443Arg
XM_011543916.1:c.1328T>G	XP_011542218.1:p.Met443Arg
XM_011543917.1:c.1127T>G	XP_011542219.1:p.Met376Arg
XM_011543918.1:c.1364T>G	XP_011542220.1:p.Met455Arg
XM_011543919.1:c.1328T>G	XP_011542221.1:p.Met443Arg
XM_017029567.1:c.1055T>G	XP_016885056.1:p.Met352Arg
NM_001114377.2:c.1004T>G	NP_001107849.1:p.Met335Arg
NM_014009.4:c.1109T>G MANE Select	NP_054728.2:p.Met370Arg