Canonical Allele Identifier: CA343471541

Gene: PBX1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.164812020C>T , CM000663.2:g.164812020C>T	GRCh38
NC_000001.10:g.164781257C>T , CM000663.1:g.164781257C>T	GRCh37
NC_000001.9:g.163047881C>T	NCBI36
NG_028246.1:g.257661C>T
NG_028246.2:g.257661C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540236.4:c.553C>T	ENSP00000439943.3:p.Arg185Trp
ENST00000699845.1:c.868C>T	ENSP00000514643.1:p.Arg290Trp
ENST00000699846.1:c.553C>T	ENSP00000514644.1:p.Arg185Trp
ENST00000699847.1:c.553C>T	ENSP00000514645.1:p.Arg185Trp
ENST00000699848.1:c.426C>T
ENST00000420696.7:c.868C>T MANE Select	ENSP00000405890.2:p.Arg290Trp
ENST00000367897.5:c.868C>T	ENSP00000356872.1:p.Arg290Trp
ENST00000420696.6:c.868C>T	ENSP00000405890.1:p.Arg290Trp
ENST00000468104.5:n.998C>T
ENST00000496120.6:n.688C>T
ENST00000540236.3:c.604C>T	ENSP00000439943.2:p.Arg202Trp
ENST00000558796.2:n.245-19451C>T
ENST00000559240.5:c.837+4343C>T	ENSP00000453188.1:n.837+4343C>T
ENST00000560469.5:n.824C>T
ENST00000560641.5:c.553C>T	ENSP00000452727.1:p.Arg185Trp
ENST00000612123.3:c.604C>T	ENSP00000483563.1:p.Arg202Trp
ENST00000627490.2:c.868C>T	ENSP00000485692.1:p.Arg290Trp
NM_001204961.1:c.868C>T	NP_001191890.1:p.Arg290Trp
NM_001204963.1:c.868C>T	NP_001191892.1:p.Arg290Trp
NM_002585.3:c.868C>T	NP_002576.1:p.Arg290Trp
XM_005245228.2:c.1036C>T	XP_005245285.1:p.Arg346Trp
XM_005245229.2:c.868C>T	XP_005245286.1:p.Arg290Trp
XM_005245230.2:c.553C>T	XP_005245287.1:p.Arg185Trp
XM_006711347.2:c.619C>T	XP_006711410.2:p.Arg207Trp
XM_011509590.1:c.1036C>T	XP_011507892.1:p.Arg346Trp
XM_011509591.1:c.1036C>T	XP_011507893.1:p.Arg346Trp
XM_011509592.1:c.1036C>T	XP_011507894.1:p.Arg346Trp
XM_011509593.1:c.688C>T	XP_011507895.1:p.Arg230Trp
XM_011509594.1:c.553C>T	XP_011507896.1:p.Arg185Trp
XM_011509595.1:c.553C>T	XP_011507897.1:p.Arg185Trp
NM_001353130.1:c.619C>T	NP_001340059.1:p.Arg207Trp
NM_001353131.1:c.868C>T	NP_001340060.1:p.Arg290Trp
XM_005245228.3:c.1036C>T	XP_005245285.1:p.Arg346Trp
XM_005245229.3:c.868C>T	XP_005245286.1:p.Arg290Trp
XM_011509590.2:c.1036C>T	XP_011507892.1:p.Arg346Trp
XM_011509591.2:c.1036C>T	XP_011507893.1:p.Arg346Trp
XM_011509592.2:c.1036C>T	XP_011507894.1:p.Arg346Trp
XM_017001395.2:c.868C>T	XP_016856884.1:p.Arg290Trp
NM_002585.4:c.868C>T MANE Select	NP_002576.1:p.Arg290Trp
NM_001204961.2:c.868C>T	NP_001191890.1:p.Arg290Trp
NM_001204963.2:c.868C>T	NP_001191892.1:p.Arg290Trp
NM_001353131.2:c.868C>T	NP_001340060.1:p.Arg290Trp