Canonical Allele Identifier: CA2580091340
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2431267
ClinVar RCV Id: RCV003140327

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621470_23621474del , CM000678.2:g.23621470_23621474del GRCh38
NC_000016.9:g.23632791_23632795del , CM000678.1:g.23632791_23632795del GRCh37
NC_000016.8:g.23540292_23540296del NCBI36
NG_007406.1:g.24887_24891del , LRG_308:g.24887_24891del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3010_3014del ENSP00000460666.3:p.Glu1004ProfsTer7
ENST00000565038.2:c.*485_*489del ENSP00000459882.2:n.*485_*489del
ENST00000566069.6:c.3004_3008del ENSP00000459237.2:p.Glu1002ProfsTer7
ENST00000697377.2:c.2848_2852del ENSP00000513286.2:p.Glu950ProfsTer7
ENST00000697379.2:c.3010_3014del ENSP00000513287.2:p.Glu1004ProfsTer7
ENST00000561514.2:c.2119_2123del ENSP00000460666.2:p.Glu707ProfsTer7
ENST00000697374.1:c.2119_2123del ENSP00000513284.1:p.Glu707ProfsTer7
ENST00000697375.1:n.4351_4355del
ENST00000697376.1:c.2119_2123del ENSP00000513285.1:p.Glu707ProfsTer7
ENST00000697377.1:c.1957_1961del ENSP00000513286.1:p.Glu653ProfsTer7
ENST00000697378.1:n.3524_3528del
ENST00000697379.1:c.2119_2123del ENSP00000513287.1:p.Glu707ProfsTer7
ENST00000697380.1:n.2296_2300del
ENST00000697381.1:n.1699_1703del
ENST00000697382.1:c.2119_2123del ENSP00000513288.1:p.Glu707ProfsTer7
ENST00000697383.1:c.538_542del ENSP00000513289.1:p.Glu180ProfsTer7
ENST00000261584.9:c.3004_3008del MANE Select ENSP00000261584.4:p.Glu1002ProfsTer7
ENST00000261584.8:c.3004_3008del ENSP00000261584.4:p.Glu1002ProfsTer7
ENST00000568219.5:c.2119_2123del ENSP00000454703.2:p.Glu707ProfsTer7
NM_024675.3:c.3004_3008del , LRG_308t1:c.3004_3008del NP_078951.2:p.Glu1002ProfsTer7
XM_011545946.1:c.3010_3014del XP_011544248.1:p.Glu1004ProfsTer7
XM_011545947.1:c.3010_3014del XP_011544249.1:p.Glu1004ProfsTer7
XM_011545948.1:c.2119_2123del XP_011544250.1:p.Glu707ProfsTer7
XR_950851.1:n.3800_3804del
XM_011545946.2:c.3010_3014del XP_011544248.1:p.Glu1004ProfsTer7
XM_011545947.2:c.3010_3014del XP_011544249.1:p.Glu1004ProfsTer7
XM_011545948.2:c.2119_2123del XP_011544250.1:p.Glu707ProfsTer7
XM_017023671.1:c.3010_3014del XP_016879160.1:p.Glu1004ProfsTer7
XM_017023672.2:c.3004_3008del XP_016879161.1:p.Glu1002ProfsTer7
XM_017023673.2:c.3004_3008del XP_016879162.1:p.Glu1002ProfsTer7
NM_024675.4:c.3004_3008del MANE Select NP_078951.2:p.Glu1002ProfsTer7