Canonical Allele Identifier: CA412951035

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49111970G>T (hg19) ; chrX:g.49255509G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49255509G>T , CM000685.2:g.49255509G>T	GRCh38
NC_000023.10:g.49111970G>T , CM000685.1:g.49111970G>T	GRCh37
NC_000023.9:g.48998914G>T	NCBI36
NG_007392.1:g.14319C>A , LRG_62:g.14319C>A
NG_021311.2:g.25045G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.631C>A	ENSP00000365372.2:p.Leu211Met
ENST00000376207.10:c.736C>A MANE Select	ENSP00000365380.4:p.Leu246Met
ENST00000455775.7:c.805C>A	ENSP00000396415.3:p.Leu269Met
ENST00000518685.6:c.735+206C>A	ENSP00000428952.2:n.735+206C>A
ENST00000557224.6:c.631C>A	ENSP00000451208.1:p.Leu211Met
ENST00000651307.1:c.736C>A	ENSP00000498454.1:p.Leu246Met
ENST00000376197.1:c.586C>A	ENSP00000365369.1:p.Leu196Met
ENST00000376199.6:c.631C>A	ENSP00000365372.2:p.Leu211Met
ENST00000376207.8:c.736C>A	ENSP00000365380.4:p.Leu246Met
ENST00000455775.6:c.805C>A	ENSP00000396415.3:p.Leu269Met
ENST00000518685.5:c.631C>A	ENSP00000428952.1:p.Leu211Met
ENST00000557224.5:c.631C>A	ENSP00000451208.1:p.Leu211Met
NM_001114377.1:c.631C>A	NP_001107849.1:p.Leu211Met
NM_014009.3:c.736C>A , LRG_62t1:c.736C>A	NP_054728.2:p.Leu246Met
XM_006724533.2:c.805C>A	XP_006724596.2:p.Leu269Met
XM_011543915.1:c.955C>A	XP_011542217.1:p.Leu319Met
XM_011543916.1:c.955C>A	XP_011542218.1:p.Leu319Met
XM_011543917.1:c.754C>A	XP_011542219.1:p.Leu252Met
XM_011543918.1:c.991C>A	XP_011542220.1:p.Leu331Met
XM_011543919.1:c.955C>A	XP_011542221.1:p.Leu319Met
XM_017029567.1:c.682C>A	XP_016885056.1:p.Leu228Met
NM_001114377.2:c.631C>A	NP_001107849.1:p.Leu211Met
NM_014009.4:c.736C>A MANE Select	NP_054728.2:p.Leu246Met