Canonical Allele Identifier: CA412950294

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49109637T>G (hg19) ; chrX:g.49253176T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49253176T>G , CM000685.2:g.49253176T>G	GRCh38
NC_000023.10:g.49109637T>G , CM000685.1:g.49109637T>G	GRCh37
NC_000023.9:g.48996581T>G	NCBI36
NG_007392.1:g.16652A>C , LRG_62:g.16652A>C
NG_021311.2:g.22712T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376199.7:c.889A>C	ENSP00000365372.2:p.Lys297Gln
ENST00000376207.10:c.994A>C MANE Select	ENSP00000365380.4:p.Lys332Gln
ENST00000455775.7:c.1063A>C	ENSP00000396415.3:p.Lys355Gln
ENST00000518685.6:c.913A>C	ENSP00000428952.2:p.Lys305Gln
ENST00000557224.6:c.889A>C	ENSP00000451208.1:p.Lys297Gln
ENST00000651307.1:c.967+741A>C	ENSP00000498454.1:n.967+741A>C
ENST00000376197.1:c.844A>C	ENSP00000365369.1:p.Lys282Gln
ENST00000376199.6:c.889A>C	ENSP00000365372.2:p.Lys297Gln
ENST00000376207.8:c.994A>C	ENSP00000365380.4:p.Lys332Gln
ENST00000455775.6:c.1063A>C	ENSP00000396415.3:p.Lys355Gln
ENST00000518685.5:c.889A>C	ENSP00000428952.1:p.Lys297Gln
ENST00000557224.5:c.889A>C	ENSP00000451208.1:p.Lys297Gln
NM_001114377.1:c.889A>C	NP_001107849.1:p.Lys297Gln
NM_014009.3:c.994A>C , LRG_62t1:c.994A>C	NP_054728.2:p.Lys332Gln
XM_006724533.2:c.1063A>C	XP_006724596.2:p.Lys355Gln
XM_011543915.1:c.1213A>C	XP_011542217.1:p.Lys405Gln
XM_011543916.1:c.1213A>C	XP_011542218.1:p.Lys405Gln
XM_011543917.1:c.1012A>C	XP_011542219.1:p.Lys338Gln
XM_011543918.1:c.1249A>C	XP_011542220.1:p.Lys417Gln
XM_011543919.1:c.1213A>C	XP_011542221.1:p.Lys405Gln
XM_017029567.1:c.940A>C	XP_016885056.1:p.Lys314Gln
NM_001114377.2:c.889A>C	NP_001107849.1:p.Lys297Gln
NM_014009.4:c.994A>C MANE Select	NP_054728.2:p.Lys332Gln