Canonical Allele Identifier: CA412947024

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49107813G>C (hg19) ; chrX:g.49251352G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251352G>C , CM000685.2:g.49251352G>C	GRCh38
NC_000023.10:g.49107813G>C , CM000685.1:g.49107813G>C	GRCh37
NC_000023.9:g.48994757G>C	NCBI36
NG_007392.1:g.18476C>G , LRG_62:g.18476C>G
NG_021311.2:g.20888G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.1173C>G	ENSP00000365372.2:p.Asn391Lys
ENST00000376207.10:c.1278C>G MANE Select	ENSP00000365380.4:p.Asn426Lys
ENST00000455775.7:c.1347C>G	ENSP00000396415.3:p.Asn449Lys
ENST00000518685.6:c.1197C>G	ENSP00000428952.2:p.Asn399Lys
ENST00000557224.6:c.1353C>G	ENSP00000451208.1:p.Asn451Lys
ENST00000651307.1:c.*193C>G	ENSP00000498454.1:n.*193C>G
ENST00000376197.1:c.1308C>G	ENSP00000365369.1:p.Asn436Lys
ENST00000376199.6:c.1173C>G	ENSP00000365372.2:p.Asn391Lys
ENST00000376207.8:c.1278C>G	ENSP00000365380.4:p.Asn426Lys
ENST00000455775.6:c.1347C>G	ENSP00000396415.3:p.Asn449Lys
ENST00000518685.5:c.1173C>G	ENSP00000428952.1:p.Asn391Lys
ENST00000557224.5:c.1353C>G	ENSP00000451208.1:p.Asn451Lys
NM_001114377.1:c.1173C>G	NP_001107849.1:p.Asn391Lys
NM_014009.3:c.1278C>G , LRG_62t1:c.1278C>G	NP_054728.2:p.Asn426Lys
XM_006724533.2:c.1347C>G	XP_006724596.2:p.Asn449Lys
XM_011543915.1:c.1677C>G	XP_011542217.1:p.Asn559Lys
XM_011543916.1:c.1677C>G	XP_011542218.1:p.Asn559Lys
XM_011543917.1:c.1296C>G	XP_011542219.1:p.Asn432Lys
XM_011543918.1:c.1533C>G	XP_011542220.1:p.Asn511Lys
XM_011543919.1:c.1497C>G	XP_011542221.1:p.Asn499Lys
XM_017029567.1:c.1404C>G	XP_016885056.1:p.Asn468Lys
NM_001114377.2:c.1173C>G	NP_001107849.1:p.Asn391Lys
NM_014009.4:c.1278C>G MANE Select	NP_054728.2:p.Asn426Lys