Canonical Allele Identifier: CA2573152181
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23635237dup , CM000678.2:g.23635237dup GRCh38
NC_000016.9:g.23646558dup , CM000678.1:g.23646558dup GRCh37
NC_000016.8:g.23554059dup NCBI36
NG_007406.1:g.11126dup , LRG_308:g.11126dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.1320dup ENSP00000460666.3:p.Gly441ArgfsTer3
ENST00000565038.2:c.211+2618dup ENSP00000459882.2:n.211+2618dup
ENST00000566069.6:c.1314dup ENSP00000459237.2:p.Gly439ArgfsTer3
ENST00000697377.2:c.1320dup ENSP00000513286.2:p.Gly441ArgfsTer3
ENST00000697379.2:c.1320dup ENSP00000513287.2:p.Gly441ArgfsTer3
ENST00000561514.2:c.429dup ENSP00000460666.2:p.Gly144ArgfsTer3
ENST00000697374.1:c.429dup ENSP00000513284.1:p.Gly144ArgfsTer3
ENST00000697375.1:n.2661dup
ENST00000697376.1:c.429dup ENSP00000513285.1:p.Gly144ArgfsTer3
ENST00000697377.1:c.429dup ENSP00000513286.1:p.Gly144ArgfsTer3
ENST00000697378.1:n.1834dup
ENST00000697379.1:c.429dup ENSP00000513287.1:p.Gly144ArgfsTer3
ENST00000697382.1:c.429dup ENSP00000513288.1:p.Gly144ArgfsTer3
ENST00000697383.1:c.48+5878dup ENSP00000513289.1:n.48+5878dup
ENST00000697384.1:n.1468dup
ENST00000261584.9:c.1314dup MANE Select ENSP00000261584.4:p.Gly439ArgfsTer3
ENST00000261584.8:c.1314dup ENSP00000261584.4:p.Gly439ArgfsTer3
ENST00000565038.1:c.86+2618dup
ENST00000568219.5:c.429dup ENSP00000454703.2:p.Gly144ArgfsTer3
NM_024675.3:c.1314dup , LRG_308t1:c.1314dup NP_078951.2:p.Gly439ArgfsTer3
XM_011545946.1:c.1320dup XP_011544248.1:p.Gly441ArgfsTer3
XM_011545947.1:c.1320dup XP_011544249.1:p.Gly441ArgfsTer3
XM_011545948.1:c.429dup XP_011544250.1:p.Gly144ArgfsTer3
XR_950851.1:n.2110dup
XM_011545946.2:c.1320dup XP_011544248.1:p.Gly441ArgfsTer3
XM_011545947.2:c.1320dup XP_011544249.1:p.Gly441ArgfsTer3
XM_011545948.2:c.429dup XP_011544250.1:p.Gly144ArgfsTer3
XM_017023671.1:c.1320dup XP_016879160.1:p.Gly441ArgfsTer3
XM_017023672.2:c.1314dup XP_016879161.1:p.Gly439ArgfsTer3
XM_017023673.2:c.1314dup XP_016879162.1:p.Gly439ArgfsTer3
NM_024675.4:c.1314dup MANE Select NP_078951.2:p.Gly439ArgfsTer3