Canonical Allele Identifier: CA915943651

Gene: PBX1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.164792620del , CM000663.2:g.164792620del	GRCh38
NC_000001.10:g.164761857del , CM000663.1:g.164761857del	GRCh37
NC_000001.9:g.163028481del	NCBI36
NG_028246.1:g.238261del
NG_028246.2:g.238261del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540236.4:c.77del	ENSP00000439943.3:p.Ala26GlufsTer?
ENST00000699845.1:c.392del	ENSP00000514643.1:p.Ala131GlufsTer?
ENST00000699846.1:c.77del	ENSP00000514644.1:p.Ala26GlufsTer?
ENST00000699847.1:c.77del	ENSP00000514645.1:p.Ala26GlufsTer?
ENST00000420696.7:c.392del MANE Select	ENSP00000405890.2:p.Ala131GlufsTer?
ENST00000340699.7:c.392del	ENSP00000341455.3:p.Ala131GlufsTer?
ENST00000367897.5:c.392del	ENSP00000356872.1:p.Ala131GlufsTer?
ENST00000420696.6:c.392del	ENSP00000405890.1:p.Ala131GlufsTer?
ENST00000468104.5:n.522del
ENST00000482110.5:c.77del	ENSP00000453163.1:p.Ala26GlufsTer?
ENST00000496120.6:n.212del
ENST00000540236.3:c.128del	ENSP00000439943.2:p.Ala43GlufsTer?
ENST00000558796.2:n.245-38851del
ENST00000558837.5:c.77del	ENSP00000453331.1:p.Ala26GlufsTer?
ENST00000559240.5:c.392del	ENSP00000453188.1:p.Ala131GlufsTer?
ENST00000559560.1:c.77del	ENSP00000453262.1:p.Ala26GlufsTer?
ENST00000559578.1:c.176del	ENSP00000452804.1:p.Ala59GlufsTer?
ENST00000560469.5:n.348del
ENST00000560641.5:c.77del	ENSP00000452727.1:p.Ala26GlufsTer?
ENST00000612123.3:c.128del	ENSP00000483563.1:p.Ala43GlufsTer?
ENST00000627490.2:c.392del	ENSP00000485692.1:p.Ala131GlufsTer?
NM_001204961.1:c.392del	NP_001191890.1:p.Ala131GlufsTer?
NM_001204963.1:c.392del	NP_001191892.1:p.Ala131GlufsTer?
NM_002585.3:c.392del	NP_002576.1:p.Ala131GlufsTer?
XM_005245228.2:c.560del	XP_005245285.1:p.Ala187GlufsTer?
XM_005245229.2:c.392del	XP_005245286.1:p.Ala131GlufsTer?
XM_005245230.2:c.77del	XP_005245287.1:p.Ala26GlufsTer?
XM_006711347.2:c.143del	XP_006711410.2:p.Ala48GlufsTer?
XM_011509590.1:c.560del	XP_011507892.1:p.Ala187GlufsTer?
XM_011509591.1:c.560del	XP_011507893.1:p.Ala187GlufsTer?
XM_011509592.1:c.560del	XP_011507894.1:p.Ala187GlufsTer?
XM_011509593.1:c.212del	XP_011507895.1:p.Ala71GlufsTer?
XM_011509594.1:c.77del	XP_011507896.1:p.Ala26GlufsTer?
XM_011509595.1:c.77del	XP_011507897.1:p.Ala26GlufsTer?
NM_001353130.1:c.143del	NP_001340059.1:p.Ala48GlufsTer?
NM_001353131.1:c.392del	NP_001340060.1:p.Ala131GlufsTer?
XM_005245228.3:c.560del	XP_005245285.1:p.Ala187GlufsTer?
XM_005245229.3:c.392del	XP_005245286.1:p.Ala131GlufsTer?
XM_011509590.2:c.560del	XP_011507892.1:p.Ala187GlufsTer?
XM_011509591.2:c.560del	XP_011507893.1:p.Ala187GlufsTer?
XM_011509592.2:c.560del	XP_011507894.1:p.Ala187GlufsTer?
XM_017001395.2:c.392del	XP_016856884.1:p.Ala131GlufsTer?
NM_002585.4:c.392del MANE Select	NP_002576.1:p.Ala131GlufsTer?
NM_001204961.2:c.392del	NP_001191890.1:p.Ala131GlufsTer?
NM_001204963.2:c.392del	NP_001191892.1:p.Ala131GlufsTer?
NM_001353131.2:c.392del	NP_001340060.1:p.Ala131GlufsTer?