Canonical Allele Identifier: CA2648874172

Gene: PBX1

Linked Data

• gnomAD v4: 1-164799903-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.164799903G>A , CM000663.2:g.164799903G>A	GRCh38
NC_000001.10:g.164769140G>A , CM000663.1:g.164769140G>A	GRCh37
NC_000001.9:g.163035764G>A	NCBI36
NG_028246.1:g.245544G>A
NG_028246.2:g.245544G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540236.4:c.386+14G>A	ENSP00000439943.3:n.386+14G>A
ENST00000699845.1:c.701+14G>A	ENSP00000514643.1:n.701+14G>A
ENST00000699846.1:c.386+14G>A	ENSP00000514644.1:n.386+14G>A
ENST00000699847.1:c.386+14G>A	ENSP00000514645.1:n.386+14G>A
ENST00000699848.1:c.259+14G>A
ENST00000420696.7:c.701+14G>A MANE Select	ENSP00000405890.2:n.701+14G>A
ENST00000367897.5:c.701+14G>A	ENSP00000356872.1:n.701+14G>A
ENST00000420696.6:c.701+14G>A	ENSP00000405890.1:n.701+14G>A
ENST00000468104.5:n.831+14G>A
ENST00000496120.6:n.521+14G>A
ENST00000540236.3:c.437+14G>A	ENSP00000439943.2:n.437+14G>A
ENST00000558796.2:n.245-31568G>A
ENST00000558837.5:c.386+14G>A	ENSP00000453331.1:n.386+14G>A
ENST00000559240.5:c.701+14G>A	ENSP00000453188.1:n.701+14G>A
ENST00000560469.5:n.657+14G>A
ENST00000560641.5:c.386+14G>A	ENSP00000452727.1:n.386+14G>A
ENST00000612123.3:c.437+14G>A	ENSP00000483563.1:n.437+14G>A
ENST00000627490.2:c.701+14G>A	ENSP00000485692.1:n.701+14G>A
NM_001204961.1:c.701+14G>A	NP_001191890.1:n.701+14G>A
NM_001204963.1:c.701+14G>A	NP_001191892.1:n.701+14G>A
NM_002585.3:c.701+14G>A	NP_002576.1:n.701+14G>A
XM_005245228.2:c.869+14G>A	XP_005245285.1:n.869+14G>A
XM_005245229.2:c.701+14G>A	XP_005245286.1:n.701+14G>A
XM_005245230.2:c.386+14G>A	XP_005245287.1:n.386+14G>A
XM_006711347.2:c.452+14G>A	XP_006711410.2:n.452+14G>A
XM_011509590.1:c.869+14G>A	XP_011507892.1:n.869+14G>A
XM_011509591.1:c.869+14G>A	XP_011507893.1:n.869+14G>A
XM_011509592.1:c.869+14G>A	XP_011507894.1:n.869+14G>A
XM_011509593.1:c.521+14G>A	XP_011507895.1:n.521+14G>A
XM_011509594.1:c.386+14G>A	XP_011507896.1:n.386+14G>A
XM_011509595.1:c.386+14G>A	XP_011507897.1:n.386+14G>A
NM_001353130.1:c.452+14G>A	NP_001340059.1:n.452+14G>A
NM_001353131.1:c.701+14G>A	NP_001340060.1:n.701+14G>A
XM_005245228.3:c.869+14G>A	XP_005245285.1:n.869+14G>A
XM_005245229.3:c.701+14G>A	XP_005245286.1:n.701+14G>A
XM_011509590.2:c.869+14G>A	XP_011507892.1:n.869+14G>A
XM_011509591.2:c.869+14G>A	XP_011507893.1:n.869+14G>A
XM_011509592.2:c.869+14G>A	XP_011507894.1:n.869+14G>A
XM_017001395.2:c.701+14G>A	XP_016856884.1:n.701+14G>A
NM_002585.4:c.701+14G>A MANE Select	NP_002576.1:n.701+14G>A
NM_001204961.2:c.701+14G>A	NP_001191890.1:n.701+14G>A
NM_001204963.2:c.701+14G>A	NP_001191892.1:n.701+14G>A
NM_001353131.2:c.701+14G>A	NP_001340060.1:n.701+14G>A