Canonical Allele Identifier: CA2573152175
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1452100
ClinVar RCV Id: RCV002035460
dbSNP Id: rs2142327301

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621423del , CM000678.2:g.23621423del GRCh38
NC_000016.9:g.23632744del , CM000678.1:g.23632744del GRCh37
NC_000016.8:g.23540245del NCBI36
NG_007406.1:g.24935del , LRG_308:g.24935del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3058del ENSP00000460666.3:p.Glu1020ArgfsTer15
ENST00000565038.2:c.*533del ENSP00000459882.2:n.*533del
ENST00000566069.6:c.3052del ENSP00000459237.2:p.Glu1018ArgfsTer15
ENST00000697377.2:c.2896del ENSP00000513286.2:p.Glu966ArgfsTer15
ENST00000697379.2:c.3058del ENSP00000513287.2:p.Glu1020ArgfsTer15
ENST00000561514.2:c.2167del ENSP00000460666.2:p.Glu723ArgfsTer15
ENST00000697374.1:c.2167del ENSP00000513284.1:p.Glu723ArgfsTer15
ENST00000697375.1:n.4399del
ENST00000697376.1:c.2167del ENSP00000513285.1:p.Glu723ArgfsTer15
ENST00000697377.1:c.2005del ENSP00000513286.1:p.Glu669ArgfsTer15
ENST00000697378.1:n.3572del
ENST00000697379.1:c.2167del ENSP00000513287.1:p.Glu723ArgfsTer15
ENST00000697380.1:n.2344del
ENST00000697381.1:n.1747del
ENST00000697382.1:c.2167del ENSP00000513288.1:p.Glu723ArgfsTer15
ENST00000697383.1:c.586del ENSP00000513289.1:p.Glu196ArgfsTer15
ENST00000261584.9:c.3052del MANE Select ENSP00000261584.4:p.Glu1018ArgfsTer15
ENST00000261584.8:c.3052del ENSP00000261584.4:p.Glu1018ArgfsTer15
ENST00000568219.5:c.2167del ENSP00000454703.2:p.Glu723ArgfsTer15
NM_024675.3:c.3052del , LRG_308t1:c.3052del NP_078951.2:p.Glu1018ArgfsTer15
XM_011545946.1:c.3058del XP_011544248.1:p.Glu1020ArgfsTer15
XM_011545947.1:c.3058del XP_011544249.1:p.Glu1020ArgfsTer15
XM_011545948.1:c.2167del XP_011544250.1:p.Glu723ArgfsTer15
XR_950851.1:n.3848del
XM_011545946.2:c.3058del XP_011544248.1:p.Glu1020ArgfsTer15
XM_011545947.2:c.3058del XP_011544249.1:p.Glu1020ArgfsTer15
XM_011545948.2:c.2167del XP_011544250.1:p.Glu723ArgfsTer15
XM_017023671.1:c.3058del XP_016879160.1:p.Glu1020ArgfsTer15
XM_017023672.2:c.3052del XP_016879161.1:p.Glu1018ArgfsTer15
XM_017023673.2:c.3052del XP_016879162.1:p.Glu1018ArgfsTer15
NM_024675.4:c.3052del MANE Select NP_078951.2:p.Glu1018ArgfsTer15