Canonical Allele Identifier: CA412949038

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108222A>G (hg19) ; chrX:g.49251761A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251761A>G , CM000685.2:g.49251761A>G	GRCh38
NC_000023.10:g.49108222A>G , CM000685.1:g.49108222A>G	GRCh37
NC_000023.9:g.48995166A>G	NCBI36
NG_007392.1:g.18067T>C , LRG_62:g.18067T>C
NG_021311.2:g.21297A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.944T>C	ENSP00000365372.2:p.Ile315Thr
ENST00000376207.10:c.1049T>C MANE Select	ENSP00000365380.4:p.Ile350Thr
ENST00000455775.7:c.1118T>C	ENSP00000396415.3:p.Ile373Thr
ENST00000518685.6:c.968T>C	ENSP00000428952.2:p.Ile323Thr
ENST00000557224.6:c.944T>C	ENSP00000451208.1:p.Ile315Thr
ENST00000651307.1:c.972T>C	ENSP00000498454.1:p.His324=
ENST00000376197.1:c.899T>C	ENSP00000365369.1:p.Ile300Thr
ENST00000376199.6:c.944T>C	ENSP00000365372.2:p.Ile315Thr
ENST00000376207.8:c.1049T>C	ENSP00000365380.4:p.Ile350Thr
ENST00000455775.6:c.1118T>C	ENSP00000396415.3:p.Ile373Thr
ENST00000518685.5:c.944T>C	ENSP00000428952.1:p.Ile315Thr
ENST00000557224.5:c.944T>C	ENSP00000451208.1:p.Ile315Thr
NM_001114377.1:c.944T>C	NP_001107849.1:p.Ile315Thr
NM_014009.3:c.1049T>C , LRG_62t1:c.1049T>C	NP_054728.2:p.Ile350Thr
XM_006724533.2:c.1118T>C	XP_006724596.2:p.Ile373Thr
XM_011543915.1:c.1268T>C	XP_011542217.1:p.Ile423Thr
XM_011543916.1:c.1268T>C	XP_011542218.1:p.Ile423Thr
XM_011543917.1:c.1067T>C	XP_011542219.1:p.Ile356Thr
XM_011543918.1:c.1304T>C	XP_011542220.1:p.Ile435Thr
XM_011543919.1:c.1268T>C	XP_011542221.1:p.Ile423Thr
XM_017029567.1:c.995T>C	XP_016885056.1:p.Ile332Thr
NM_001114377.2:c.944T>C	NP_001107849.1:p.Ile315Thr
NM_014009.4:c.1049T>C MANE Select	NP_054728.2:p.Ile350Thr