Canonical Allele Identifier: CA279505163
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs1016313749

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23640976C>T , CM000678.2:g.23640976C>T GRCh38
NC_000016.9:g.23652297C>T , CM000678.1:g.23652297C>T GRCh37
NC_000016.8:g.23559798C>T NCBI36
NG_007406.1:g.5382G>A , LRG_308:g.5382G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.-671G>A ENSP00000460666.3:n.-671G>A
ENST00000565038.2:c.48+134G>A ENSP00000459882.2:n.48+134G>A
ENST00000566069.6:c.48+134G>A ENSP00000459237.2:n.48+134G>A
ENST00000697377.2:c.-192+134G>A ENSP00000513286.2:n.-192+134G>A
ENST00000697379.2:c.-98+134G>A ENSP00000513287.2:n.-98+134G>A
ENST00000561514.2:c.-1562G>A ENSP00000460666.2:n.-1562G>A
ENST00000697374.1:c.-1153G>A ENSP00000513284.1:n.-1153G>A
ENST00000697376.1:c.-1008+134G>A ENSP00000513285.1:n.-1008+134G>A
ENST00000697377.1:c.-1083+134G>A ENSP00000513286.1:n.-1083+134G>A
ENST00000697379.1:c.-989+134G>A ENSP00000513287.1:n.-989+134G>A
ENST00000697382.1:c.-1613G>A ENSP00000513288.1:n.-1613G>A
ENST00000697383.1:c.48+134G>A ENSP00000513289.1:n.48+134G>A
ENST00000697384.1:n.202+134G>A
ENST00000261584.9:c.48+134G>A MANE Select ENSP00000261584.4:n.48+134G>A
ENST00000261584.8:c.48+134G>A ENSP00000261584.4:n.48+134G>A
ENST00000567003.1:n.192+134G>A
ENST00000568219.5:c.-838+151G>A ENSP00000454703.2:n.-838+151G>A
NM_024675.3:c.48+134G>A , LRG_308t1:c.48+134G>A NP_078951.2:n.48+134G>A
XM_011545946.1:c.-671G>A XP_011544248.1:n.-671G>A
XM_011545947.1:c.-671G>A XP_011544249.1:n.-671G>A
XM_011545948.1:c.-972+134G>A XP_011544250.1:n.-972+134G>A
XR_950851.1:n.120G>A
XM_011545946.2:c.-671G>A XP_011544248.1:n.-671G>A
XM_011545947.2:c.-671G>A XP_011544249.1:n.-671G>A
XM_011545948.2:c.-972+134G>A XP_011544250.1:n.-972+134G>A
XM_017023671.1:c.-671G>A XP_016879160.1:n.-671G>A
XM_017023672.2:c.48+134G>A XP_016879161.1:n.48+134G>A
XM_017023673.2:c.48+134G>A XP_016879162.1:n.48+134G>A
NM_024675.4:c.48+134G>A MANE Select NP_078951.2:n.48+134G>A