Canonical Allele Identifier: CA915949211
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 822391
ClinVar RCV Id: RCV001017717
dbSNP Id: rs1597098094

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23635706del , CM000678.2:g.23635706del GRCh38
NC_000016.9:g.23647027del , CM000678.1:g.23647027del GRCh37
NC_000016.8:g.23554528del NCBI36
NG_007406.1:g.10652del , LRG_308:g.10652del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.846del ENSP00000460666.3:p.Asn282LysfsTer8
ENST00000565038.2:c.211+2144del ENSP00000459882.2:n.211+2144del
ENST00000566069.6:c.840del ENSP00000459237.2:p.Asn280LysfsTer8
ENST00000697377.2:c.846del ENSP00000513286.2:p.Asn282LysfsTer8
ENST00000697379.2:c.846del ENSP00000513287.2:p.Asn282LysfsTer8
ENST00000561514.2:c.-46del ENSP00000460666.2:n.-46del
ENST00000697374.1:c.-46del ENSP00000513284.1:n.-46del
ENST00000697375.1:n.2187del
ENST00000697376.1:c.-46del ENSP00000513285.1:n.-46del
ENST00000697377.1:c.-46del ENSP00000513286.1:n.-46del
ENST00000697378.1:n.1360del
ENST00000697379.1:c.-46del ENSP00000513287.1:n.-46del
ENST00000697382.1:c.-46del ENSP00000513288.1:n.-46del
ENST00000697383.1:c.48+5404del ENSP00000513289.1:n.48+5404del
ENST00000697384.1:n.994del
ENST00000261584.9:c.840del MANE Select ENSP00000261584.4:p.Asn280LysfsTer8
ENST00000261584.8:c.840del ENSP00000261584.4:p.Asn280LysfsTer8
ENST00000565038.1:c.86+2144del
ENST00000568219.5:c.-46del ENSP00000454703.2:n.-46del
NM_024675.3:c.840del , LRG_308t1:c.840del NP_078951.2:p.Asn280LysfsTer8
XM_011545946.1:c.846del XP_011544248.1:p.Asn282LysfsTer8
XM_011545947.1:c.846del XP_011544249.1:p.Asn282LysfsTer8
XM_011545948.1:c.-46del XP_011544250.1:n.-46del
XR_950851.1:n.1636del
XM_011545946.2:c.846del XP_011544248.1:p.Asn282LysfsTer8
XM_011545947.2:c.846del XP_011544249.1:p.Asn282LysfsTer8
XM_011545948.2:c.-46del XP_011544250.1:n.-46del
XM_017023671.1:c.846del XP_016879160.1:p.Asn282LysfsTer8
XM_017023672.2:c.840del XP_016879161.1:p.Asn280LysfsTer8
XM_017023673.2:c.840del XP_016879162.1:p.Asn280LysfsTer8
NM_024675.4:c.840del MANE Select NP_078951.2:p.Asn280LysfsTer8