Canonical Allele Identifier: CA3265662806

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23637905_23638011del , CM000678.2:g.23637905_23638011del	GRCh38
NC_000016.9:g.23649226_23649332del , CM000678.1:g.23649226_23649332del	GRCh37
NC_000016.8:g.23556727_23556833del	NCBI36
NG_007406.1:g.8347_8453del , LRG_308:g.8347_8453del

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.3:c.109-59_156del , LRG_308t1:c.109-59_156del
NM_024675.4:c.109-59_156del
ENST00000261584.8:c.109-59_156del
ENST00000261584.9:c.109-59_156del
ENST00000561514.1:c.115-59_162del
ENST00000561514.2:c.-777-59_-730del
ENST00000561514.3:c.115-59_162del
ENST00000565038.2:c.109-59_156del
ENST00000566069.6:c.109-59_156del
ENST00000567003.1:n.387-59_434del
ENST00000568219.5:c.-777-59_-730del
ENST00000697374.1:c.-777-59_-730del
ENST00000697375.1:n.1456-59_1503del
ENST00000697376.1:c.-813-23_-730del
ENST00000697377.1:c.-777-59_-730del
ENST00000697377.2:c.115-59_162del
ENST00000697378.1:n.629-59_676del
ENST00000697379.1:c.-777-59_-730del
ENST00000697379.2:c.115-59_162del
ENST00000697382.1:c.-777-59_-730del
ENST00000697383.1:c.48+3099_48+3205del	ENSP00000513289.1:n.48+3099_48+3205del
ENST00000697384.1:n.263-59_310del
XM_011545946.1:c.115-59_162del
XM_011545946.2:c.115-59_162del
XM_011545947.1:c.115-59_162del
XM_011545947.2:c.115-59_162del
XM_011545948.1:c.-777-59_-730del
XM_011545948.2:c.-777-59_-730del
XM_017023671.1:c.115-59_162del
XM_017023672.2:c.109-59_156del
XM_017023673.2:c.109-59_156del
XR_950851.1:n.905-59_952del