Canonical Allele Identifier: CA10617368

Gene: FOXP1

Linked Data

• ClinVar Variation Id: 346563
• ClinVar RCV Id: RCV000387309
• dbSNP Id: rs143202281
• gnomAD v2: 3-71004983-G-GCA
• gnomAD v3: 3-70955832-G-GCA
• gnomAD v4: 3-70955832-G-GCA
• MyVariant Identifiers: chr3:g.71004984_71004985dupCA (hg19) ; chr3:g.71004985_71004986insCA (hg19) ; chr3:g.71004983_71004984insCA (hg19) ; chr3:g.70955833_70955834dupCA (hg38) ; chr3:g.70955834_70955835insCA (hg38) ; chr3:g.70955832_70955833insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.70955855_70955856dup , CM000665.2:g.70955855_70955856dup	GRCh38
NC_000003.11:g.71005006_71005007dup , CM000665.1:g.71005006_71005007dup	GRCh37
NC_000003.10:g.71087696_71087697dup	NCBI36
NG_028243.1:g.633156_633157dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000318789.11:c.*3413_*3414dup	ENSP00000318902.5:n.*3413_*3414dup
ENST00000318789.10:c.*3413_*3414dup	ENSP00000318902.5:n.*3413_*3414dup
ENST00000649528.3:c.*3413_*3414dup MANE Select	ENSP00000497369.1:n.*3413_*3414dup
ENST00000674446.1:c.*3413_*3414dup	ENSP00000501439.1:n.*3413_*3414dup
ENST00000318789.8:c.*3413_*3414dup	ENSP00000318902.4:n.*3413_*3414dup
ENST00000614176.4:c.*3413_*3414dup	ENSP00000482847.1:n.*3413_*3414dup
ENST00000615603.4:c.*3413_*3414dup	ENSP00000484803.1:n.*3413_*3414dup
NM_001244808.1:c.*3413_*3414dup	NP_001231737.1:n.*3413_*3414dup
NM_001244810.1:c.*3413_*3414dup	NP_001231739.1:n.*3413_*3414dup
NM_001244812.1:c.*3413_*3414dup	NP_001231741.1:n.*3413_*3414dup
NM_001244813.1:c.*3413_*3414dup	NP_001231742.1:n.*3413_*3414dup
NM_001244814.1:c.*3413_*3414dup	NP_001231743.1:n.*3413_*3414dup
NM_001244815.1:c.*3413_*3414dup	NP_001231744.1:n.*3413_*3414dup
NM_001244816.1:c.*3413_*3414dup	NP_001231745.1:n.*3413_*3414dup
NM_032682.5:c.*3413_*3414dup	NP_116071.2:n.*3413_*3414dup
XM_005264735.2:c.*3413_*3414dup	XP_005264792.1:n.*3413_*3414dup
XM_005264736.2:c.*3413_*3414dup	XP_005264793.1:n.*3413_*3414dup
XM_005264742.2:c.*3413_*3414dup	XP_005264799.1:n.*3413_*3414dup
XM_006713102.1:c.*3413_*3414dup	XP_006713165.1:n.*3413_*3414dup
XM_006713103.1:c.*3413_*3414dup	XP_006713166.1:n.*3413_*3414dup
XM_006713104.1:c.*3413_*3414dup	XP_006713167.1:n.*3413_*3414dup
XM_011533585.1:c.*3413_*3414dup	XP_011531887.1:n.*3413_*3414dup
XM_011533587.1:c.*3413_*3414dup	XP_011531889.1:n.*3413_*3414dup
XM_011533588.1:c.*3413_*3414dup	XP_011531890.1:n.*3413_*3414dup
XR_427266.2:n.9279_9280dup
XR_940413.1:n.5881_5882dup
XR_940414.1:n.9429_9430dup
NM_001349337.1:c.*3413_*3414dup	NP_001336266.1:n.*3413_*3414dup
NM_001349338.1:c.*3413_*3414dup	NP_001336267.1:n.*3413_*3414dup
NM_001349340.1:c.*3413_*3414dup	NP_001336269.1:n.*3413_*3414dup
NM_001349341.1:c.*3413_*3414dup	NP_001336270.1:n.*3413_*3414dup
NM_001349342.1:c.*3413_*3414dup	NP_001336271.1:n.*3413_*3414dup
NM_001349343.1:c.*3413_*3414dup	NP_001336272.1:n.*3413_*3414dup
NM_001349344.1:c.*3413_*3414dup	NP_001336273.1:n.*3413_*3414dup
NR_146142.1:n.5988_5989dup
NR_146143.1:n.5985_5986dup
NM_001244808.2:c.*3413_*3414dup	NP_001231737.1:n.*3413_*3414dup
NM_001244812.2:c.*3413_*3414dup	NP_001231741.1:n.*3413_*3414dup
NM_001244813.2:c.*3413_*3414dup	NP_001231742.1:n.*3413_*3414dup
NM_001244814.2:c.*3413_*3414dup	NP_001231743.1:n.*3413_*3414dup
NM_001244815.2:c.*3413_*3414dup	NP_001231744.2:n.*3413_*3414dup
NM_001349337.2:c.*3413_*3414dup	NP_001336266.2:n.*3413_*3414dup
NM_001349338.2:c.*3413_*3414dup	NP_001336267.1:n.*3413_*3414dup
NM_001349340.2:c.*3413_*3414dup	NP_001336269.1:n.*3413_*3414dup
NM_001349341.2:c.*3413_*3414dup	NP_001336270.1:n.*3413_*3414dup
NM_001349342.2:c.*3413_*3414dup	NP_001336271.1:n.*3413_*3414dup
NM_001349343.2:c.*3413_*3414dup	NP_001336272.1:n.*3413_*3414dup
NM_001349344.2:c.*3413_*3414dup	NP_001336273.1:n.*3413_*3414dup
NM_001370548.1:c.*3413_*3414dup	NP_001357477.1:n.*3413_*3414dup
NM_032682.6:c.*3413_*3414dup	NP_116071.2:n.*3413_*3414dup
NR_146142.2:n.5963_5964dup
NR_146143.2:n.5960_5961dup
NM_001244808.3:c.*3413_*3414dup	NP_001231737.1:n.*3413_*3414dup
NM_001244810.2:c.*3413_*3414dup	NP_001231739.1:n.*3413_*3414dup
NM_001244812.3:c.*3413_*3414dup	NP_001231741.1:n.*3413_*3414dup
NM_001244813.3:c.*3413_*3414dup	NP_001231742.1:n.*3413_*3414dup
NM_001244814.3:c.*3413_*3414dup	NP_001231743.1:n.*3413_*3414dup
NM_001244816.2:c.*3413_*3414dup	NP_001231745.1:n.*3413_*3414dup
NM_001349338.3:c.*3413_*3414dup MANE Select	NP_001336267.1:n.*3413_*3414dup
NM_001349340.3:c.*3413_*3414dup	NP_001336269.1:n.*3413_*3414dup
NM_001349341.3:c.*3413_*3414dup	NP_001336270.1:n.*3413_*3414dup
NM_001349342.3:c.*3413_*3414dup	NP_001336271.1:n.*3413_*3414dup
NM_001349343.3:c.*3413_*3414dup	NP_001336272.1:n.*3413_*3414dup
NM_001349344.3:c.*3413_*3414dup	NP_001336273.1:n.*3413_*3414dup
NR_146142.3:n.5963_5964dup
NR_146143.3:n.5960_5961dup