Canonical Allele Identifier: CA1219291

Gene: PBX1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.164559883G>A , CM000663.2:g.164559883G>A	GRCh38
NC_000001.10:g.164529120G>A , CM000663.1:g.164529120G>A	GRCh37
NC_000001.9:g.162795744G>A	NCBI36
NG_028246.1:g.5524G>A
NG_028246.2:g.5524G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002585.4:c.61G>A MANE Select	NP_002576.1:p.Gly21Ser
ENST00000420696.7:c.61G>A MANE Select	ENSP00000405890.2:p.Gly21Ser
NM_001204961.1:c.61G>A	NP_001191890.1:p.Gly21Ser
NM_001204961.2:c.61G>A	NP_001191890.1:p.Gly21Ser
NM_001204963.1:c.61G>A	NP_001191892.1:p.Gly21Ser
NM_001204963.2:c.61G>A	NP_001191892.1:p.Gly21Ser
NM_001353130.1:c.-115G>A	NP_001340059.1:n.-115G>A
NM_001353131.1:c.61G>A	NP_001340060.1:p.Gly21Ser
NM_001353131.2:c.61G>A	NP_001340060.1:p.Gly21Ser
NM_002585.3:c.61G>A	NP_002576.1:p.Gly21Ser
ENST00000340699.7:c.61G>A	ENSP00000341455.3:p.Gly21Ser
ENST00000367897.5:c.61G>A	ENSP00000356872.1:p.Gly21Ser
ENST00000420696.6:c.61G>A	ENSP00000405890.1:p.Gly21Ser
ENST00000467023.5:n.137-3355G>A
ENST00000485769.5:c.61G>A	ENSP00000473998.1:p.Gly21Ser
ENST00000498497.2:n.61G>A
ENST00000559240.5:c.61G>A	ENSP00000453188.1:p.Gly21Ser
ENST00000627490.2:c.61G>A	ENSP00000485692.1:p.Gly21Ser
ENST00000699845.1:c.61G>A	ENSP00000514643.1:p.Gly21Ser
XM_005245228.2:c.61G>A	XP_005245285.1:p.Gly21Ser
XM_005245228.3:c.61G>A	XP_005245285.1:p.Gly21Ser
XM_005245229.2:c.61G>A	XP_005245286.1:p.Gly21Ser
XM_005245229.3:c.61G>A	XP_005245286.1:p.Gly21Ser
XM_011509590.1:c.61G>A	XP_011507892.1:p.Gly21Ser
XM_011509590.2:c.61G>A	XP_011507892.1:p.Gly21Ser
XM_011509591.1:c.61G>A	XP_011507893.1:p.Gly21Ser
XM_011509591.2:c.61G>A	XP_011507893.1:p.Gly21Ser
XM_011509592.1:c.61G>A	XP_011507894.1:p.Gly21Ser
XM_011509592.2:c.61G>A	XP_011507894.1:p.Gly21Ser
XM_011509596.1:c.61G>A	XP_011507898.1:p.Gly21Ser
XM_017001395.2:c.61G>A	XP_016856884.1:p.Gly21Ser