Canonical Allele Identifier: CA2580613440

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23612793_23619928dup , CM000678.2:g.23612793_23619928dup	GRCh38

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3119+1434_3207+1211dup
ENST00000565038.2:c.*594+1434_*682+1211dup
ENST00000566069.6:c.3113+1434_3201+1211dup
ENST00000697377.2:c.2957+1434_3045+1211dup
ENST00000697379.2:c.3119+1434_3207+1211dup
ENST00000561514.2:c.2228+1434_2316+1211dup
ENST00000697374.1:c.2228+1434_2316+1211dup
ENST00000697375.1:n.4460+1434_4548+1211dup
ENST00000697376.1:c.2228+1434_2316+1211dup
ENST00000697377.1:c.2066+1434_2154+1211dup
ENST00000697378.1:n.3633+1434_3721+1211dup
ENST00000697379.1:c.2228+1434_2316+1211dup
ENST00000697380.1:n.2405+1434_2406-4781dup
ENST00000697381.1:n.1808+1434_1896+1211dup
ENST00000697382.1:c.2228+1434_2229-4781dup	ENSP00000513288.1:n.2228+1434_2229-4781du...
ENST00000697383.1:c.647+1434_735+1211dup
ENST00000261584.9:c.3113+1434_3201+1211dup
ENST00000261584.8:c.3113+1434_3201+1211dup
ENST00000566069.5:c.28+1434_116+1211dup
ENST00000568219.5:c.2228+1434_2316+1211dup
NM_024675.3:c.3113+1434_3201+1211dup , LRG_308t1:c.3113+1434_3201+1211dup
XM_011545946.1:c.3119+1434_3207+1211dup
XM_011545947.1:c.3119+1434_3207+1211dup
XM_011545948.1:c.2228+1434_2316+1211dup
XR_950851.1:n.3909+1434_3910-4781dup
XM_011545946.2:c.3119+1434_3207+1211dup
XM_011545947.2:c.3119+1434_3207+1211dup
XM_011545948.2:c.2228+1434_2316+1211dup
XM_017023671.1:c.3119+1434_3119+8569dup	XP_016879160.1:n.3119+1434_3119+8569dup
XM_017023672.2:c.3113+1434_3113+8569dup	XP_016879161.1:n.3113+1434_3113+8569dup
XM_017023673.2:c.3113+1434_3201+1211dup
NM_024675.4:c.3113+1434_3201+1211dup