Canonical Allele Identifier: CA2697555709
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2702376

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621398dup , CM000678.2:g.23621398dup GRCh38
NC_000016.9:g.23632719dup , CM000678.1:g.23632719dup GRCh37
NC_000016.8:g.23540220dup NCBI36
NG_007406.1:g.24960dup , LRG_308:g.24960dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3083dup ENSP00000460666.3:p.Leu1029AlafsTer26
ENST00000565038.2:c.*558dup ENSP00000459882.2:n.*558dup
ENST00000566069.6:c.3077dup ENSP00000459237.2:p.Leu1027AlafsTer26
ENST00000697377.2:c.2921dup ENSP00000513286.2:p.Leu975AlafsTer26
ENST00000697379.2:c.3083dup ENSP00000513287.2:p.Leu1029AlafsTer26
ENST00000561514.2:c.2192dup ENSP00000460666.2:p.Leu732AlafsTer26
ENST00000697374.1:c.2192dup ENSP00000513284.1:p.Leu732AlafsTer26
ENST00000697375.1:n.4424dup
ENST00000697376.1:c.2192dup ENSP00000513285.1:p.Leu732AlafsTer26
ENST00000697377.1:c.2030dup ENSP00000513286.1:p.Leu678AlafsTer26
ENST00000697378.1:n.3597dup
ENST00000697379.1:c.2192dup ENSP00000513287.1:p.Leu732AlafsTer26
ENST00000697380.1:n.2369dup
ENST00000697381.1:n.1772dup
ENST00000697382.1:c.2192dup ENSP00000513288.1:p.Leu732AlafsTer?
ENST00000697383.1:c.611dup ENSP00000513289.1:p.Leu205AlafsTer26
ENST00000261584.9:c.3077dup MANE Select ENSP00000261584.4:p.Leu1027AlafsTer26
ENST00000261584.8:c.3077dup ENSP00000261584.4:p.Leu1027AlafsTer26
ENST00000568219.5:c.2192dup ENSP00000454703.2:p.Leu732AlafsTer26
NM_024675.3:c.3077dup , LRG_308t1:c.3077dup NP_078951.2:p.Leu1027AlafsTer26
XM_011545946.1:c.3083dup XP_011544248.1:p.Leu1029AlafsTer26
XM_011545947.1:c.3083dup XP_011544249.1:p.Leu1029AlafsTer26
XM_011545948.1:c.2192dup XP_011544250.1:p.Leu732AlafsTer26
XR_950851.1:n.3873dup
XM_011545946.2:c.3083dup XP_011544248.1:p.Leu1029AlafsTer26
XM_011545947.2:c.3083dup XP_011544249.1:p.Leu1029AlafsTer26
XM_011545948.2:c.2192dup XP_011544250.1:p.Leu732AlafsTer26
XM_017023671.1:c.3083dup XP_016879160.1:p.Leu1029AlafsTer17
XM_017023672.2:c.3077dup XP_016879161.1:p.Leu1027AlafsTer17
XM_017023673.2:c.3077dup XP_016879162.1:p.Leu1027AlafsTer26
NM_024675.4:c.3077dup MANE Select NP_078951.2:p.Leu1027AlafsTer26