Canonical Allele Identifier: CA1139768301
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2816092
ClinVar RCV Id: RCV003607906

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621484_23621485del , CM000678.2:g.23621484_23621485del GRCh38
NC_000016.9:g.23632805_23632806del , CM000678.1:g.23632805_23632806del GRCh37
NC_000016.8:g.23540306_23540307del NCBI36
NG_007406.1:g.24873_24874del , LRG_308:g.24873_24874del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3003-7_3003-6del ENSP00000460666.3:n.3003-7_3003-6del
ENST00000565038.2:c.*478-7_*478-6del ENSP00000459882.2:n.*478-7_*478-6del
ENST00000566069.6:c.2997-7_2997-6del ENSP00000459237.2:n.2997-7_2997-6del
ENST00000697377.2:c.2841-7_2841-6del ENSP00000513286.2:n.2841-7_2841-6del
ENST00000697379.2:c.3003-7_3003-6del ENSP00000513287.2:n.3003-7_3003-6del
ENST00000561514.2:c.2112-7_2112-6del ENSP00000460666.2:n.2112-7_2112-6del
ENST00000697374.1:c.2112-7_2112-6del ENSP00000513284.1:n.2112-7_2112-6del
ENST00000697375.1:n.4344-7_4344-6del
ENST00000697376.1:c.2112-7_2112-6del ENSP00000513285.1:n.2112-7_2112-6del
ENST00000697377.1:c.1950-7_1950-6del ENSP00000513286.1:n.1950-7_1950-6del
ENST00000697378.1:n.3517-7_3517-6del
ENST00000697379.1:c.2112-7_2112-6del ENSP00000513287.1:n.2112-7_2112-6del
ENST00000697380.1:n.2289-7_2289-6del
ENST00000697381.1:n.1692-7_1692-6del
ENST00000697382.1:c.2112-7_2112-6del ENSP00000513288.1:n.2112-7_2112-6del
ENST00000697383.1:c.531-7_531-6del ENSP00000513289.1:n.531-7_531-6del
ENST00000261584.9:c.2997-7_2997-6del MANE Select ENSP00000261584.4:n.2997-7_2997-6del
ENST00000261584.8:c.2997-7_2997-6del ENSP00000261584.4:n.2997-7_2997-6del
ENST00000568219.5:c.2112-7_2112-6del ENSP00000454703.2:n.2112-7_2112-6del
NM_024675.3:c.2997-7_2997-6del , LRG_308t1:c.2997-7_2997-6del NP_078951.2:n.2997-7_2997-6del
XM_011545946.1:c.3003-7_3003-6del XP_011544248.1:n.3003-7_3003-6del
XM_011545947.1:c.3003-7_3003-6del XP_011544249.1:n.3003-7_3003-6del
XM_011545948.1:c.2112-7_2112-6del XP_011544250.1:n.2112-7_2112-6del
XR_950851.1:n.3793-7_3793-6del
XM_011545946.2:c.3003-7_3003-6del XP_011544248.1:n.3003-7_3003-6del
XM_011545947.2:c.3003-7_3003-6del XP_011544249.1:n.3003-7_3003-6del
XM_011545948.2:c.2112-7_2112-6del XP_011544250.1:n.2112-7_2112-6del
XM_017023671.1:c.3003-7_3003-6del XP_016879160.1:n.3003-7_3003-6del
XM_017023672.2:c.2997-7_2997-6del XP_016879161.1:n.2997-7_2997-6del
XM_017023673.2:c.2997-7_2997-6del XP_016879162.1:n.2997-7_2997-6del
NM_024675.4:c.2997-7_2997-6del MANE Select NP_078951.2:n.2997-7_2997-6del