Canonical Allele Identifier: CA2695197621
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2677465
ClinVar RCV Id: RCV003476612

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23641136_23641140del , CM000678.2:g.23641136_23641140del GRCh38
NC_000016.9:g.23652457_23652461del , CM000678.1:g.23652457_23652461del GRCh37
NC_000016.8:g.23559958_23559962del NCBI36
NG_007406.1:g.5218_5222del , LRG_308:g.5218_5222del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.-835_-831del ENSP00000460666.3:n.-835_-831del
ENST00000565038.2:c.18_22del ENSP00000459882.2:p.Lys7ProfsTer4
ENST00000566069.6:c.18_22del ENSP00000459237.2:p.Lys7ProfsTer4
ENST00000697377.2:c.-222_-218del ENSP00000513286.2:n.-222_-218del
ENST00000697379.2:c.-128_-124del ENSP00000513287.2:n.-128_-124del
ENST00000561514.2:c.-1726_-1722del ENSP00000460666.2:n.-1726_-1722del
ENST00000697374.1:c.-1317_-1313del ENSP00000513284.1:n.-1317_-1313del
ENST00000697376.1:c.-1038_-1034del ENSP00000513285.1:n.-1038_-1034del
ENST00000697377.1:c.-1113_-1109del ENSP00000513286.1:n.-1113_-1109del
ENST00000697379.1:c.-1019_-1015del ENSP00000513287.1:n.-1019_-1015del
ENST00000697382.1:c.-1777_-1773del ENSP00000513288.1:n.-1777_-1773del
ENST00000697383.1:c.18_22del ENSP00000513289.1:p.Lys7ProfsTer4
ENST00000697384.1:n.172_176del
ENST00000261584.9:c.18_22del MANE Select ENSP00000261584.4:p.Lys7ProfsTer4
ENST00000261584.8:c.18_22del ENSP00000261584.4:p.Lys7ProfsTer4
ENST00000567003.1:n.162_166del
ENST00000568219.5:c.-851_-847del ENSP00000454703.2:n.-851_-847del
NM_024675.3:c.18_22del , LRG_308t1:c.18_22del NP_078951.2:p.Lys7ProfsTer4
XM_011545948.1:c.-1002_-998del XP_011544250.1:n.-1002_-998del
XM_011545946.2:c.-835_-831del XP_011544248.1:n.-835_-831del
XM_011545947.2:c.-835_-831del XP_011544249.1:n.-835_-831del
XM_011545948.2:c.-1002_-998del XP_011544250.1:n.-1002_-998del
XM_017023671.1:c.-835_-831del XP_016879160.1:n.-835_-831del
XM_017023672.2:c.18_22del XP_016879161.1:p.Lys7ProfsTer4
XM_017023673.2:c.18_22del XP_016879162.1:p.Lys7ProfsTer4
NM_024675.4:c.18_22del MANE Select NP_078951.2:p.Lys7ProfsTer4