Canonical Allele Identifier: CA412950931

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49111925C>G (hg19) ; chrX:g.49255464C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255464C>G , CM000685.2:g.49255464C>G	GRCh38
NC_000023.10:g.49111925C>G , CM000685.1:g.49111925C>G	GRCh37
NC_000023.9:g.48998869C>G	NCBI36
NG_007392.1:g.14364G>C , LRG_62:g.14364G>C
NG_021311.2:g.25000C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.676G>C	ENSP00000365372.2:p.Ala226Pro
ENST00000376207.10:c.781G>C MANE Select	ENSP00000365380.4:p.Ala261Pro
ENST00000455775.7:c.850G>C	ENSP00000396415.3:p.Ala284Pro
ENST00000518685.6:c.735+251G>C	ENSP00000428952.2:n.735+251G>C
ENST00000557224.6:c.676G>C	ENSP00000451208.1:p.Ala226Pro
ENST00000651307.1:c.781G>C	ENSP00000498454.1:p.Ala261Pro
ENST00000376197.1:c.631G>C	ENSP00000365369.1:p.Ala211Pro
ENST00000376199.6:c.676G>C	ENSP00000365372.2:p.Ala226Pro
ENST00000376207.8:c.781G>C	ENSP00000365380.4:p.Ala261Pro
ENST00000455775.6:c.850G>C	ENSP00000396415.3:p.Ala284Pro
ENST00000518685.5:c.676G>C	ENSP00000428952.1:p.Ala226Pro
ENST00000557224.5:c.676G>C	ENSP00000451208.1:p.Ala226Pro
NM_001114377.1:c.676G>C	NP_001107849.1:p.Ala226Pro
NM_014009.3:c.781G>C , LRG_62t1:c.781G>C	NP_054728.2:p.Ala261Pro
XM_006724533.2:c.850G>C	XP_006724596.2:p.Ala284Pro
XM_011543915.1:c.1000G>C	XP_011542217.1:p.Ala334Pro
XM_011543916.1:c.1000G>C	XP_011542218.1:p.Ala334Pro
XM_011543917.1:c.799G>C	XP_011542219.1:p.Ala267Pro
XM_011543918.1:c.1036G>C	XP_011542220.1:p.Ala346Pro
XM_011543919.1:c.1000G>C	XP_011542221.1:p.Ala334Pro
XM_017029567.1:c.727G>C	XP_016885056.1:p.Ala243Pro
NM_001114377.2:c.676G>C	NP_001107849.1:p.Ala226Pro
NM_014009.4:c.781G>C MANE Select	NP_054728.2:p.Ala261Pro