Canonical Allele Identifier: CA11409519

Gene: FOXP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.71251416A>G , CM000665.2:g.71251416A>G	GRCh38
NC_000003.11:g.71300567A>G , CM000665.1:g.71300567A>G	GRCh37
NC_000003.10:g.71383257A>G	NCBI36
NG_028243.1:g.337574T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318789.11:c.-12+48404T>C	ENSP00000318902.5:n.-12+48404T>C
ENST00000615603.5:n.420+48404T>C
ENST00000648710.2:c.-12+48404T>C	ENSP00000497430.2:n.-12+48404T>C
ENST00000649431.2:c.-12+48404T>C	ENSP00000498174.2:n.-12+48404T>C
ENST00000649610.2:c.-12+48404T>C	ENSP00000497693.2:n.-12+48404T>C
ENST00000650068.2:c.-12+48404T>C	ENSP00000497454.2:n.-12+48404T>C
ENST00000318789.10:c.-12+48404T>C	ENSP00000318902.5:n.-12+48404T>C
ENST00000327590.9:c.-12+48404T>C	ENSP00000333560.4:n.-12+48404T>C
ENST00000471386.3:c.-12+48404T>C	ENSP00000497992.1:n.-12+48404T>C
ENST00000493089.7:c.-12+48404T>C	ENSP00000418524.1:n.-12+48404T>C
ENST00000610810.5:c.-12+48404T>C	ENSP00000479663.2:n.-12+48404T>C
ENST00000647614.1:c.-19+45017T>C	ENSP00000497710.1:n.-19+45017T>C
ENST00000647725.1:c.-12+48404T>C	ENSP00000497585.1:n.-12+48404T>C
ENST00000648107.1:c.-12+38127T>C	ENSP00000497914.1:n.-12+38127T>C
ENST00000648321.1:c.-12+48404T>C	ENSP00000498015.1:n.-12+48404T>C
ENST00000648380.1:c.-12+48404T>C	ENSP00000497344.1:n.-12+48404T>C
ENST00000648384.1:c.-12+48404T>C	ENSP00000497976.1:n.-12+48404T>C
ENST00000648662.1:c.-12+36899T>C	ENSP00000496873.1:n.-12+36899T>C
ENST00000648710.1:c.-12+48404T>C	ENSP00000497430.1:n.-12+48404T>C
ENST00000648718.1:c.-12+48404T>C	ENSP00000496810.1:n.-12+48404T>C
ENST00000648783.1:c.-12+48404T>C	ENSP00000498063.1:n.-12+48404T>C
ENST00000648826.1:n.230+45017T>C
ENST00000648895.1:c.-12+48404T>C	ENSP00000497417.1:n.-12+48404T>C
ENST00000648944.1:c.-12+45017T>C	ENSP00000497405.1:n.-12+45017T>C
ENST00000649431.1:c.-12+45017T>C	ENSP00000498174.1:n.-12+45017T>C
ENST00000649513.1:c.-154+48404T>C	ENSP00000497237.1:n.-154+48404T>C
ENST00000649528.3:c.-12+48404T>C MANE Select	ENSP00000497369.1:n.-12+48404T>C
ENST00000649596.1:c.-12+48404T>C	ENSP00000496932.1:n.-12+48404T>C
ENST00000649610.1:c.-12+45017T>C	ENSP00000497693.1:n.-12+45017T>C
ENST00000649631.1:c.-12+48404T>C	ENSP00000496990.1:n.-12+48404T>C
ENST00000650068.1:c.-12+48404T>C	ENSP00000497454.1:n.-12+48404T>C
ENST00000650123.1:c.507+48404T>C
ENST00000650156.1:c.-12+48404T>C	ENSP00000496852.1:n.-12+48404T>C
ENST00000650295.1:c.-12+48404T>C	ENSP00000497138.1:n.-12+48404T>C
ENST00000318779.7:c.-12+48404T>C	ENSP00000318721.3:n.-12+48404T>C
ENST00000318789.8:c.-12+48404T>C	ENSP00000318902.4:n.-12+48404T>C
ENST00000327590.8:c.-12+48404T>C	ENSP00000333560.4:n.-12+48404T>C
ENST00000475937.5:c.-12+48404T>C	ENSP00000419393.1:n.-12+48404T>C
ENST00000484350.5:c.-12+48404T>C	ENSP00000417857.1:n.-12+48404T>C
ENST00000493089.5:c.-12+48404T>C	ENSP00000418524.1:n.-12+48404T>C
ENST00000610810.4:c.-12+48404T>C	ENSP00000479663.1:n.-12+48404T>C
ENST00000615603.4:c.-12+48404T>C	ENSP00000484803.1:n.-12+48404T>C
NM_001012505.1:c.-12+48404T>C	NP_001012523.1:n.-12+48404T>C
NM_001244808.1:c.-12+48404T>C	NP_001231737.1:n.-12+48404T>C
NM_001244810.1:c.-12+48404T>C	NP_001231739.1:n.-12+48404T>C
NM_001244812.1:c.-12+48404T>C	NP_001231741.1:n.-12+48404T>C
NM_001244816.1:c.-12+48404T>C	NP_001231745.1:n.-12+48404T>C
NM_032682.5:c.-12+48404T>C	NP_116071.2:n.-12+48404T>C
XM_005264737.3:c.-12+48404T>C	XP_005264794.1:n.-12+48404T>C
XM_006713102.1:c.-12+48404T>C	XP_006713165.1:n.-12+48404T>C
XM_006713103.1:c.-12+48404T>C	XP_006713166.1:n.-12+48404T>C
XM_006713104.1:c.-12+48404T>C	XP_006713167.1:n.-12+48404T>C
XM_011533584.1:c.-12+48404T>C	XP_011531886.1:n.-12+48404T>C
XM_011533585.1:c.-12+48404T>C	XP_011531887.1:n.-12+48404T>C
XM_011533586.1:c.-12+48404T>C	XP_011531888.1:n.-12+48404T>C
XM_011533587.1:c.-12+38127T>C	XP_011531889.1:n.-12+38127T>C
XR_427266.2:n.3651+48404T>C
XR_940414.1:n.3801+48404T>C
NM_001349338.1:c.-12+48404T>C	NP_001336267.1:n.-12+48404T>C
NM_001349340.1:c.-12+48404T>C	NP_001336269.1:n.-12+48404T>C
NM_001349341.1:c.-12+48404T>C	NP_001336270.1:n.-12+48404T>C
NR_146142.1:n.618+48404T>C
NR_146143.1:n.618+48404T>C
XM_006713102.2:c.-12+48404T>C	XP_006713165.1:n.-12+48404T>C
XM_006713103.2:c.-12+48404T>C	XP_006713166.1:n.-12+48404T>C
XM_006713104.2:c.-12+48404T>C	XP_006713167.1:n.-12+48404T>C
XM_011533585.3:c.-12+48404T>C	XP_011531887.1:n.-12+48404T>C
XM_017006165.1:c.-12+48404T>C	XP_016861654.1:n.-12+48404T>C
XM_017006168.2:c.-12+48404T>C	XP_016861657.1:n.-12+48404T>C
NM_001244808.2:c.-12+48404T>C	NP_001231737.1:n.-12+48404T>C
NM_001244812.2:c.-12+48404T>C	NP_001231741.1:n.-12+48404T>C
NM_001349338.2:c.-12+48404T>C	NP_001336267.1:n.-12+48404T>C
NM_001349340.2:c.-12+48404T>C	NP_001336269.1:n.-12+48404T>C
NM_001349341.2:c.-12+48404T>C	NP_001336270.1:n.-12+48404T>C
NM_032682.6:c.-12+48404T>C	NP_116071.2:n.-12+48404T>C
NR_146142.2:n.593+48404T>C
NR_146143.2:n.593+48404T>C
NM_001012505.2:c.-12+48404T>C	NP_001012523.1:n.-12+48404T>C
NM_001244808.3:c.-12+48404T>C	NP_001231737.1:n.-12+48404T>C
NM_001244810.2:c.-12+48404T>C	NP_001231739.1:n.-12+48404T>C
NM_001244812.3:c.-12+48404T>C	NP_001231741.1:n.-12+48404T>C
NM_001244816.2:c.-12+48404T>C	NP_001231745.1:n.-12+48404T>C
NM_001349338.3:c.-12+48404T>C MANE Select	NP_001336267.1:n.-12+48404T>C
NM_001349340.3:c.-12+48404T>C	NP_001336269.1:n.-12+48404T>C
NM_001349341.3:c.-12+48404T>C	NP_001336270.1:n.-12+48404T>C
NR_146142.3:n.593+48404T>C
NR_146143.3:n.593+48404T>C