Canonical Allele Identifier: CA2213436315

Gene: PALB2

Linked Data

• dbSNP Id: rs1360779670

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23640979dup , CM000678.2:g.23640979dup	GRCh38
NC_000016.9:g.23652300dup , CM000678.1:g.23652300dup	GRCh37
NC_000016.8:g.23559801dup	NCBI36
NG_007406.1:g.5383dup , LRG_308:g.5383dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-670dup	ENSP00000460666.3:n.-670dup
ENST00000565038.2:c.48+135dup	ENSP00000459882.2:n.48+135dup
ENST00000566069.6:c.48+135dup	ENSP00000459237.2:n.48+135dup
ENST00000697377.2:c.-192+135dup	ENSP00000513286.2:n.-192+135dup
ENST00000697379.2:c.-98+135dup	ENSP00000513287.2:n.-98+135dup
ENST00000561514.2:c.-1561dup	ENSP00000460666.2:n.-1561dup
ENST00000697374.1:c.-1152dup	ENSP00000513284.1:n.-1152dup
ENST00000697376.1:c.-1008+135dup	ENSP00000513285.1:n.-1008+135dup
ENST00000697377.1:c.-1083+135dup	ENSP00000513286.1:n.-1083+135dup
ENST00000697379.1:c.-989+135dup	ENSP00000513287.1:n.-989+135dup
ENST00000697382.1:c.-1612dup	ENSP00000513288.1:n.-1612dup
ENST00000697383.1:c.48+135dup	ENSP00000513289.1:n.48+135dup
ENST00000697384.1:n.202+135dup
ENST00000261584.9:c.48+135dup MANE Select	ENSP00000261584.4:n.48+135dup
ENST00000261584.8:c.48+135dup	ENSP00000261584.4:n.48+135dup
ENST00000567003.1:n.192+135dup
ENST00000568219.5:c.-838+152dup	ENSP00000454703.2:n.-838+152dup
NM_024675.3:c.48+135dup , LRG_308t1:c.48+135dup	NP_078951.2:n.48+135dup
XM_011545946.1:c.-670dup	XP_011544248.1:n.-670dup
XM_011545947.1:c.-670dup	XP_011544249.1:n.-670dup
XM_011545948.1:c.-972+135dup	XP_011544250.1:n.-972+135dup
XR_950851.1:n.121dup
XM_011545946.2:c.-670dup	XP_011544248.1:n.-670dup
XM_011545947.2:c.-670dup	XP_011544249.1:n.-670dup
XM_011545948.2:c.-972+135dup	XP_011544250.1:n.-972+135dup
XM_017023671.1:c.-670dup	XP_016879160.1:n.-670dup
XM_017023672.2:c.48+135dup	XP_016879161.1:n.48+135dup
XM_017023673.2:c.48+135dup	XP_016879162.1:n.48+135dup
NM_024675.4:c.48+135dup MANE Select	NP_078951.2:n.48+135dup