Canonical Allele Identifier: CA412950984

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49111948A>G (hg19) ; chrX:g.49255487A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255487A>G , CM000685.2:g.49255487A>G	GRCh38
NC_000023.10:g.49111948A>G , CM000685.1:g.49111948A>G	GRCh37
NC_000023.9:g.48998892A>G	NCBI36
NG_007392.1:g.14341T>C , LRG_62:g.14341T>C
NG_021311.2:g.25023A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.653T>C	ENSP00000365372.2:p.Leu218Pro
ENST00000376207.10:c.758T>C MANE Select	ENSP00000365380.4:p.Leu253Pro
ENST00000455775.7:c.827T>C	ENSP00000396415.3:p.Leu276Pro
ENST00000518685.6:c.735+228T>C	ENSP00000428952.2:n.735+228T>C
ENST00000557224.6:c.653T>C	ENSP00000451208.1:p.Leu218Pro
ENST00000651307.1:c.758T>C	ENSP00000498454.1:p.Leu253Pro
ENST00000376197.1:c.608T>C	ENSP00000365369.1:p.Leu203Pro
ENST00000376199.6:c.653T>C	ENSP00000365372.2:p.Leu218Pro
ENST00000376207.8:c.758T>C	ENSP00000365380.4:p.Leu253Pro
ENST00000455775.6:c.827T>C	ENSP00000396415.3:p.Leu276Pro
ENST00000518685.5:c.653T>C	ENSP00000428952.1:p.Leu218Pro
ENST00000557224.5:c.653T>C	ENSP00000451208.1:p.Leu218Pro
NM_001114377.1:c.653T>C	NP_001107849.1:p.Leu218Pro
NM_014009.3:c.758T>C , LRG_62t1:c.758T>C	NP_054728.2:p.Leu253Pro
XM_006724533.2:c.827T>C	XP_006724596.2:p.Leu276Pro
XM_011543915.1:c.977T>C	XP_011542217.1:p.Leu326Pro
XM_011543916.1:c.977T>C	XP_011542218.1:p.Leu326Pro
XM_011543917.1:c.776T>C	XP_011542219.1:p.Leu259Pro
XM_011543918.1:c.1013T>C	XP_011542220.1:p.Leu338Pro
XM_011543919.1:c.977T>C	XP_011542221.1:p.Leu326Pro
XM_017029567.1:c.704T>C	XP_016885056.1:p.Leu235Pro
NM_001114377.2:c.653T>C	NP_001107849.1:p.Leu218Pro
NM_014009.4:c.758T>C MANE Select	NP_054728.2:p.Leu253Pro