Canonical Allele Identifier: CA516569820

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251441G>T , CM000685.2:g.49251441G>T	GRCh38
NC_000023.10:g.49107902G>T , CM000685.1:g.49107902G>T	GRCh37
NC_000023.9:g.48994846G>T	NCBI36
NG_007392.1:g.18387C>A , LRG_62:g.18387C>A
NG_021311.2:g.20977G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.1084C>A	ENSP00000365372.2:p.Arg362=
ENST00000376207.10:c.1189C>A MANE Select	ENSP00000365380.4:p.Arg397=
ENST00000455775.7:c.1258C>A	ENSP00000396415.3:p.Arg420=
ENST00000518685.6:c.1108C>A	ENSP00000428952.2:p.Arg370=
ENST00000557224.6:c.1264C>A	ENSP00000451208.1:p.Arg422=
ENST00000651307.1:c.*104C>A	ENSP00000498454.1:n.*104C>A
ENST00000376197.1:c.1219C>A	ENSP00000365369.1:p.Arg407=
ENST00000376199.6:c.1084C>A	ENSP00000365372.2:p.Arg362=
ENST00000376207.8:c.1189C>A	ENSP00000365380.4:p.Arg397=
ENST00000455775.6:c.1258C>A	ENSP00000396415.3:p.Arg420=
ENST00000518685.5:c.1084C>A	ENSP00000428952.1:p.Arg362=
ENST00000557224.5:c.1264C>A	ENSP00000451208.1:p.Arg422=
NM_001114377.1:c.1084C>A	NP_001107849.1:p.Arg362=
NM_014009.3:c.1189C>A , LRG_62t1:c.1189C>A	NP_054728.2:p.Arg397=
XM_006724533.2:c.1258C>A	XP_006724596.2:p.Arg420=
XM_011543915.1:c.1588C>A	XP_011542217.1:p.Arg530=
XM_011543916.1:c.1588C>A	XP_011542218.1:p.Arg530=
XM_011543917.1:c.1207C>A	XP_011542219.1:p.Arg403=
XM_011543918.1:c.1444C>A	XP_011542220.1:p.Arg482=
XM_011543919.1:c.1408C>A	XP_011542221.1:p.Arg470=
XM_017029567.1:c.1315C>A	XP_016885056.1:p.Arg439=
NM_001114377.2:c.1084C>A	NP_001107849.1:p.Arg362=
NM_014009.4:c.1189C>A MANE Select	NP_054728.2:p.Arg397=