Canonical Allele Identifier: CA2580613444
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2567573

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621401dup , CM000678.2:g.23621401dup GRCh38
NC_000016.9:g.23632722dup , CM000678.1:g.23632722dup GRCh37
NC_000016.8:g.23540223dup NCBI36
NG_007406.1:g.24957dup , LRG_308:g.24957dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3080dup ENSP00000460666.3:p.Leu1028SerfsTer27
ENST00000565038.2:c.*555dup ENSP00000459882.2:n.*555dup
ENST00000566069.6:c.3074dup ENSP00000459237.2:p.Leu1026SerfsTer27
ENST00000697377.2:c.2918dup ENSP00000513286.2:p.Leu974SerfsTer27
ENST00000697379.2:c.3080dup ENSP00000513287.2:p.Leu1028SerfsTer27
ENST00000561514.2:c.2189dup ENSP00000460666.2:p.Leu731SerfsTer27
ENST00000697374.1:c.2189dup ENSP00000513284.1:p.Leu731SerfsTer27
ENST00000697375.1:n.4421dup
ENST00000697376.1:c.2189dup ENSP00000513285.1:p.Leu731SerfsTer27
ENST00000697377.1:c.2027dup ENSP00000513286.1:p.Leu677SerfsTer27
ENST00000697378.1:n.3594dup
ENST00000697379.1:c.2189dup ENSP00000513287.1:p.Leu731SerfsTer27
ENST00000697380.1:n.2366dup
ENST00000697381.1:n.1769dup
ENST00000697382.1:c.2189dup ENSP00000513288.1:p.Leu731SerfsTer?
ENST00000697383.1:c.608dup ENSP00000513289.1:p.Leu204SerfsTer27
ENST00000261584.9:c.3074dup MANE Select ENSP00000261584.4:p.Leu1026SerfsTer27
ENST00000261584.8:c.3074dup ENSP00000261584.4:p.Leu1026SerfsTer27
ENST00000568219.5:c.2189dup ENSP00000454703.2:p.Leu731SerfsTer27
NM_024675.3:c.3074dup , LRG_308t1:c.3074dup NP_078951.2:p.Leu1026SerfsTer27
XM_011545946.1:c.3080dup XP_011544248.1:p.Leu1028SerfsTer27
XM_011545947.1:c.3080dup XP_011544249.1:p.Leu1028SerfsTer27
XM_011545948.1:c.2189dup XP_011544250.1:p.Leu731SerfsTer27
XR_950851.1:n.3870dup
XM_011545946.2:c.3080dup XP_011544248.1:p.Leu1028SerfsTer27
XM_011545947.2:c.3080dup XP_011544249.1:p.Leu1028SerfsTer27
XM_011545948.2:c.2189dup XP_011544250.1:p.Leu731SerfsTer27
XM_017023671.1:c.3080dup XP_016879160.1:p.Leu1028SerfsTer18
XM_017023672.2:c.3074dup XP_016879161.1:p.Leu1026SerfsTer18
XM_017023673.2:c.3074dup XP_016879162.1:p.Leu1026SerfsTer27
NM_024675.4:c.3074dup MANE Select NP_078951.2:p.Leu1026SerfsTer27