Canonical Allele Identifier: CA196785
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 187120
dbSNP Id: rs786203488

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621471_23621474del , CM000678.2:g.23621471_23621474del GRCh38
NC_000016.9:g.23632792_23632795del , CM000678.1:g.23632792_23632795del GRCh37
NC_000016.8:g.23540293_23540296del NCBI36
NG_007406.1:g.24887_24890del , LRG_308:g.24887_24890del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3010_3013del ENSP00000460666.3:p.Glu1004ThrfsTer4
ENST00000565038.2:c.*485_*488del ENSP00000459882.2:n.*485_*488del
ENST00000566069.6:c.3004_3007del ENSP00000459237.2:p.Glu1002ThrfsTer4
ENST00000697377.2:c.2848_2851del ENSP00000513286.2:p.Glu950ThrfsTer4
ENST00000697379.2:c.3010_3013del ENSP00000513287.2:p.Glu1004ThrfsTer4
ENST00000561514.2:c.2119_2122del ENSP00000460666.2:p.Glu707ThrfsTer4
ENST00000697374.1:c.2119_2122del ENSP00000513284.1:p.Glu707ThrfsTer4
ENST00000697375.1:n.4351_4354del
ENST00000697376.1:c.2119_2122del ENSP00000513285.1:p.Glu707ThrfsTer4
ENST00000697377.1:c.1957_1960del ENSP00000513286.1:p.Glu653ThrfsTer4
ENST00000697378.1:n.3524_3527del
ENST00000697379.1:c.2119_2122del ENSP00000513287.1:p.Glu707ThrfsTer4
ENST00000697380.1:n.2296_2299del
ENST00000697381.1:n.1699_1702del
ENST00000697382.1:c.2119_2122del ENSP00000513288.1:p.Glu707ThrfsTer4
ENST00000697383.1:c.538_541del ENSP00000513289.1:p.Glu180ThrfsTer4
ENST00000261584.9:c.3004_3007del MANE Select ENSP00000261584.4:p.Glu1002ThrfsTer4
ENST00000261584.8:c.3004_3007del ENSP00000261584.4:p.Glu1002ThrfsTer4
ENST00000568219.5:c.2119_2122del ENSP00000454703.2:p.Glu707ThrfsTer4
NM_024675.3:c.3004_3007del , LRG_308t1:c.3004_3007del NP_078951.2:p.Glu1002ThrfsTer4
XM_011545946.1:c.3010_3013del XP_011544248.1:p.Glu1004ThrfsTer4
XM_011545947.1:c.3010_3013del XP_011544249.1:p.Glu1004ThrfsTer4
XM_011545948.1:c.2119_2122del XP_011544250.1:p.Glu707ThrfsTer4
XR_950851.1:n.3800_3803del
XM_011545946.2:c.3010_3013del XP_011544248.1:p.Glu1004ThrfsTer4
XM_011545947.2:c.3010_3013del XP_011544249.1:p.Glu1004ThrfsTer4
XM_011545948.2:c.2119_2122del XP_011544250.1:p.Glu707ThrfsTer4
XM_017023671.1:c.3010_3013del XP_016879160.1:p.Glu1004ThrfsTer4
XM_017023672.2:c.3004_3007del XP_016879161.1:p.Glu1002ThrfsTer4
XM_017023673.2:c.3004_3007del XP_016879162.1:p.Glu1002ThrfsTer4
NM_024675.4:c.3004_3007del MANE Select NP_078951.2:p.Glu1002ThrfsTer4