Canonical Allele Identifier: CA648303015

Gene: FOXP1

Linked Data

• COSMIC: COSN24372028

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.70957417_70957418insC , CM000665.2:g.70957417_70957418insC	GRCh38
NC_000003.11:g.71006568_71006569insC , CM000665.1:g.71006568_71006569insC	GRCh37
NC_000003.10:g.71089258_71089259insC	NCBI36
NG_028243.1:g.631572_631573insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318789.11:c.*1829_*1830insG	ENSP00000318902.5:n.*1829_*1830insG
ENST00000615603.5:n.4294_4295insG
ENST00000318789.10:c.*1829_*1830insG	ENSP00000318902.5:n.*1829_*1830insG
ENST00000649528.3:c.*1829_*1830insG MANE Select	ENSP00000497369.1:n.*1829_*1830insG
ENST00000674446.1:c.*1829_*1830insG	ENSP00000501439.1:n.*1829_*1830insG
ENST00000318789.8:c.*1829_*1830insG	ENSP00000318902.4:n.*1829_*1830insG
ENST00000475937.5:c.*1829_*1830insG	ENSP00000419393.1:n.*1829_*1830insG
ENST00000614176.4:c.*1829_*1830insG	ENSP00000482847.1:n.*1829_*1830insG
ENST00000615603.4:c.*1829_*1830insG	ENSP00000484803.1:n.*1829_*1830insG
NM_001244808.1:c.*1829_*1830insG	NP_001231737.1:n.*1829_*1830insG
NM_001244810.1:c.*1829_*1830insG	NP_001231739.1:n.*1829_*1830insG
NM_001244812.1:c.*1829_*1830insG	NP_001231741.1:n.*1829_*1830insG
NM_001244813.1:c.*1829_*1830insG	NP_001231742.1:n.*1829_*1830insG
NM_001244814.1:c.*1829_*1830insG	NP_001231743.1:n.*1829_*1830insG
NM_001244815.1:c.*1829_*1830insG	NP_001231744.1:n.*1829_*1830insG
NM_001244816.1:c.*1829_*1830insG	NP_001231745.1:n.*1829_*1830insG
NM_032682.5:c.*1829_*1830insG	NP_116071.2:n.*1829_*1830insG
XM_005264735.2:c.*1829_*1830insG	XP_005264792.1:n.*1829_*1830insG
XM_005264736.2:c.*1829_*1830insG	XP_005264793.1:n.*1829_*1830insG
XM_005264737.3:c.*1829_*1830insG	XP_005264794.1:n.*1829_*1830insG
XM_005264742.2:c.*1829_*1830insG	XP_005264799.1:n.*1829_*1830insG
XM_006713102.1:c.*1829_*1830insG	XP_006713165.1:n.*1829_*1830insG
XM_006713103.1:c.*1829_*1830insG	XP_006713166.1:n.*1829_*1830insG
XM_006713104.1:c.*1829_*1830insG	XP_006713167.1:n.*1829_*1830insG
XM_011533584.1:c.*1829_*1830insG	XP_011531886.1:n.*1829_*1830insG
XM_011533585.1:c.*1829_*1830insG	XP_011531887.1:n.*1829_*1830insG
XM_011533586.1:c.*1829_*1830insG	XP_011531888.1:n.*1829_*1830insG
XM_011533587.1:c.*1829_*1830insG	XP_011531889.1:n.*1829_*1830insG
XM_011533588.1:c.*1829_*1830insG	XP_011531890.1:n.*1829_*1830insG
XR_427266.2:n.7695_7696insG
XR_940413.1:n.4297_4298insG
XR_940414.1:n.7845_7846insG
NM_001349337.1:c.*1829_*1830insG	NP_001336266.1:n.*1829_*1830insG
NM_001349338.1:c.*1829_*1830insG	NP_001336267.1:n.*1829_*1830insG
NM_001349340.1:c.*1829_*1830insG	NP_001336269.1:n.*1829_*1830insG
NM_001349341.1:c.*1829_*1830insG	NP_001336270.1:n.*1829_*1830insG
NM_001349342.1:c.*1829_*1830insG	NP_001336271.1:n.*1829_*1830insG
NM_001349343.1:c.*1829_*1830insG	NP_001336272.1:n.*1829_*1830insG
NM_001349344.1:c.*1829_*1830insG	NP_001336273.1:n.*1829_*1830insG
NR_146142.1:n.4404_4405insG
NR_146143.1:n.4401_4402insG
XM_006713102.2:c.*1829_*1830insG	XP_006713165.1:n.*1829_*1830insG
XM_011533585.3:c.*1829_*1830insG	XP_011531887.1:n.*1829_*1830insG
XM_017006165.1:c.*1829_*1830insG	XP_016861654.1:n.*1829_*1830insG
NM_001244808.2:c.*1829_*1830insG	NP_001231737.1:n.*1829_*1830insG
NM_001244812.2:c.*1829_*1830insG	NP_001231741.1:n.*1829_*1830insG
NM_001244813.2:c.*1829_*1830insG	NP_001231742.1:n.*1829_*1830insG
NM_001244814.2:c.*1829_*1830insG	NP_001231743.1:n.*1829_*1830insG
NM_001244815.2:c.*1829_*1830insG	NP_001231744.2:n.*1829_*1830insG
NM_001349337.2:c.*1829_*1830insG	NP_001336266.2:n.*1829_*1830insG
NM_001349338.2:c.*1829_*1830insG	NP_001336267.1:n.*1829_*1830insG
NM_001349340.2:c.*1829_*1830insG	NP_001336269.1:n.*1829_*1830insG
NM_001349341.2:c.*1829_*1830insG	NP_001336270.1:n.*1829_*1830insG
NM_001349342.2:c.*1829_*1830insG	NP_001336271.1:n.*1829_*1830insG
NM_001349343.2:c.*1829_*1830insG	NP_001336272.1:n.*1829_*1830insG
NM_001349344.2:c.*1829_*1830insG	NP_001336273.1:n.*1829_*1830insG
NM_001370548.1:c.*1829_*1830insG	NP_001357477.1:n.*1829_*1830insG
NM_032682.6:c.*1829_*1830insG	NP_116071.2:n.*1829_*1830insG
NR_146142.2:n.4379_4380insG
NR_146143.2:n.4376_4377insG
NM_001244808.3:c.*1829_*1830insG	NP_001231737.1:n.*1829_*1830insG
NM_001244810.2:c.*1829_*1830insG	NP_001231739.1:n.*1829_*1830insG
NM_001244812.3:c.*1829_*1830insG	NP_001231741.1:n.*1829_*1830insG
NM_001244813.3:c.*1829_*1830insG	NP_001231742.1:n.*1829_*1830insG
NM_001244814.3:c.*1829_*1830insG	NP_001231743.1:n.*1829_*1830insG
NM_001244816.2:c.*1829_*1830insG	NP_001231745.1:n.*1829_*1830insG
NM_001349338.3:c.*1829_*1830insG MANE Select	NP_001336267.1:n.*1829_*1830insG
NM_001349340.3:c.*1829_*1830insG	NP_001336269.1:n.*1829_*1830insG
NM_001349341.3:c.*1829_*1830insG	NP_001336270.1:n.*1829_*1830insG
NM_001349342.3:c.*1829_*1830insG	NP_001336271.1:n.*1829_*1830insG
NM_001349343.3:c.*1829_*1830insG	NP_001336272.1:n.*1829_*1830insG
NM_001349344.3:c.*1829_*1830insG	NP_001336273.1:n.*1829_*1830insG
NR_146142.3:n.4379_4380insG
NR_146143.3:n.4376_4377insG