Canonical Allele Identifier: CA891844511
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 584903
ClinVar RCV Id: RCV000989552
dbSNP Id: rs1567213009

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621470del , CM000678.2:g.23621470del GRCh38
NC_000016.9:g.23632791del , CM000678.1:g.23632791del GRCh37
NC_000016.8:g.23540292del NCBI36
NG_007406.1:g.24891del , LRG_308:g.24891del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3014del ENSP00000460666.3:p.Asn1005ThrfsTer4
ENST00000565038.2:c.*489del ENSP00000459882.2:n.*489del
ENST00000566069.6:c.3008del ENSP00000459237.2:p.Asn1003ThrfsTer4
ENST00000697377.2:c.2852del ENSP00000513286.2:p.Asn951ThrfsTer4
ENST00000697379.2:c.3014del ENSP00000513287.2:p.Asn1005ThrfsTer4
ENST00000561514.2:c.2123del ENSP00000460666.2:p.Asn708ThrfsTer4
ENST00000697374.1:c.2123del ENSP00000513284.1:p.Asn708ThrfsTer4
ENST00000697375.1:n.4355del
ENST00000697376.1:c.2123del ENSP00000513285.1:p.Asn708ThrfsTer4
ENST00000697377.1:c.1961del ENSP00000513286.1:p.Asn654ThrfsTer4
ENST00000697378.1:n.3528del
ENST00000697379.1:c.2123del ENSP00000513287.1:p.Asn708ThrfsTer4
ENST00000697380.1:n.2300del
ENST00000697381.1:n.1703del
ENST00000697382.1:c.2123del ENSP00000513288.1:p.Asn708ThrfsTer4
ENST00000697383.1:c.542del ENSP00000513289.1:p.Asn181ThrfsTer4
ENST00000261584.9:c.3008del MANE Select ENSP00000261584.4:p.Asn1003ThrfsTer4
ENST00000261584.8:c.3008del ENSP00000261584.4:p.Asn1003ThrfsTer4
ENST00000568219.5:c.2123del ENSP00000454703.2:p.Asn708ThrfsTer4
NM_024675.3:c.3008del , LRG_308t1:c.3008del NP_078951.2:p.Asn1003ThrfsTer4
XM_011545946.1:c.3014del XP_011544248.1:p.Asn1005ThrfsTer4
XM_011545947.1:c.3014del XP_011544249.1:p.Asn1005ThrfsTer4
XM_011545948.1:c.2123del XP_011544250.1:p.Asn708ThrfsTer4
XR_950851.1:n.3804del
XM_011545946.2:c.3014del XP_011544248.1:p.Asn1005ThrfsTer4
XM_011545947.2:c.3014del XP_011544249.1:p.Asn1005ThrfsTer4
XM_011545948.2:c.2123del XP_011544250.1:p.Asn708ThrfsTer4
XM_017023671.1:c.3014del XP_016879160.1:p.Asn1005ThrfsTer4
XM_017023672.2:c.3008del XP_016879161.1:p.Asn1003ThrfsTer4
XM_017023673.2:c.3008del XP_016879162.1:p.Asn1003ThrfsTer4
NM_024675.4:c.3008del MANE Select NP_078951.2:p.Asn1003ThrfsTer4