Canonical Allele Identifier: CA412948954

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108198C>G (hg19) ; chrX:g.49251737C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251737C>G , CM000685.2:g.49251737C>G	GRCh38
NC_000023.10:g.49108198C>G , CM000685.1:g.49108198C>G	GRCh37
NC_000023.9:g.48995142C>G	NCBI36
NG_007392.1:g.18091G>C , LRG_62:g.18091G>C
NG_021311.2:g.21273C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.968G>C	ENSP00000365372.2:p.Arg323Pro
ENST00000376207.10:c.1073G>C MANE Select	ENSP00000365380.4:p.Arg358Pro
ENST00000455775.7:c.1142G>C	ENSP00000396415.3:p.Arg381Pro
ENST00000518685.6:c.992G>C	ENSP00000428952.2:p.Arg331Pro
ENST00000557224.6:c.968G>C	ENSP00000451208.1:p.Arg323Pro
ENST00000651307.1:c.996G>C	ENSP00000498454.1:p.Ala332=
ENST00000376197.1:c.923G>C	ENSP00000365369.1:p.Arg308Pro
ENST00000376199.6:c.968G>C	ENSP00000365372.2:p.Arg323Pro
ENST00000376207.8:c.1073G>C	ENSP00000365380.4:p.Arg358Pro
ENST00000455775.6:c.1142G>C	ENSP00000396415.3:p.Arg381Pro
ENST00000518685.5:c.968G>C	ENSP00000428952.1:p.Arg323Pro
ENST00000557224.5:c.968G>C	ENSP00000451208.1:p.Arg323Pro
NM_001114377.1:c.968G>C	NP_001107849.1:p.Arg323Pro
NM_014009.3:c.1073G>C , LRG_62t1:c.1073G>C	NP_054728.2:p.Arg358Pro
XM_006724533.2:c.1142G>C	XP_006724596.2:p.Arg381Pro
XM_011543915.1:c.1292G>C	XP_011542217.1:p.Arg431Pro
XM_011543916.1:c.1292G>C	XP_011542218.1:p.Arg431Pro
XM_011543917.1:c.1091G>C	XP_011542219.1:p.Arg364Pro
XM_011543918.1:c.1328G>C	XP_011542220.1:p.Arg443Pro
XM_011543919.1:c.1292G>C	XP_011542221.1:p.Arg431Pro
XM_017029567.1:c.1019G>C	XP_016885056.1:p.Arg340Pro
NM_001114377.2:c.968G>C	NP_001107849.1:p.Arg323Pro
NM_014009.4:c.1073G>C MANE Select	NP_054728.2:p.Arg358Pro