Canonical Allele Identifier: CA412948239

Gene: FOXP3

Linked Data

• MyVariant Identifiers: chrX:g.49108054C>G (hg19) ; chrX:g.49251593C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49251593C>G , CM000685.2:g.49251593C>G	GRCh38
NC_000023.10:g.49108054C>G , CM000685.1:g.49108054C>G	GRCh37
NC_000023.9:g.48994998C>G	NCBI36
NG_007392.1:g.18235G>C , LRG_62:g.18235G>C
NG_021311.2:g.21129C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376199.7:c.1041+71G>C	ENSP00000365372.2:n.1041+71G>C
ENST00000376207.10:c.1146+71G>C MANE Select	ENSP00000365380.4:n.1146+71G>C
ENST00000455775.7:c.1215+71G>C	ENSP00000396415.3:n.1215+71G>C
ENST00000518685.6:c.1065+71G>C	ENSP00000428952.2:n.1065+71G>C
ENST00000557224.6:c.1112G>C	ENSP00000451208.1:p.Trp371Ser
ENST00000651307.1:c.*61+71G>C	ENSP00000498454.1:n.*61+71G>C
ENST00000376197.1:c.1067G>C	ENSP00000365369.1:p.Trp356Ser
ENST00000376199.6:c.1041+71G>C	ENSP00000365372.2:n.1041+71G>C
ENST00000376207.8:c.1146+71G>C	ENSP00000365380.4:n.1146+71G>C
ENST00000455775.6:c.1215+71G>C	ENSP00000396415.3:n.1215+71G>C
ENST00000518685.5:c.1041+71G>C	ENSP00000428952.1:n.1041+71G>C
ENST00000557224.5:c.1112G>C	ENSP00000451208.1:p.Trp371Ser
NM_001114377.1:c.1041+71G>C	NP_001107849.1:n.1041+71G>C
NM_014009.3:c.1146+71G>C , LRG_62t1:c.1146+71G>C	NP_054728.2:n.1146+71G>C
XM_006724533.2:c.1215+71G>C	XP_006724596.2:n.1215+71G>C
XM_011543915.1:c.1436G>C	XP_011542217.1:p.Trp479Ser
XM_011543916.1:c.1436G>C	XP_011542218.1:p.Trp479Ser
XM_011543917.1:c.1164+71G>C	XP_011542219.1:n.1164+71G>C
XM_011543918.1:c.1401+71G>C	XP_011542220.1:n.1401+71G>C
XM_011543919.1:c.1365+71G>C	XP_011542221.1:n.1365+71G>C
XM_017029567.1:c.1163G>C	XP_016885056.1:p.Trp388Ser
NM_001114377.2:c.1041+71G>C	NP_001107849.1:n.1041+71G>C
NM_014009.4:c.1146+71G>C MANE Select	NP_054728.2:n.1146+71G>C