Canonical Allele Identifier: CA2850447222

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23637852_23637954del , CM000678.2:g.23637852_23637954del	GRCh38
NC_000016.9:g.23649173_23649275del , CM000678.1:g.23649173_23649275del	GRCh37
NC_000016.8:g.23556674_23556776del	NCBI36
NG_007406.1:g.8406_8508del , LRG_308:g.8406_8508del

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.3:c.109_211del , LRG_308t1:c.109_211del
NM_024675.4:c.109_211del
ENST00000261584.8:c.109_211del
ENST00000261584.9:c.109_211del
ENST00000561514.1:c.115_217del
ENST00000561514.2:c.-777_-675del
ENST00000561514.3:c.115_217del
ENST00000565038.2:c.109_211del
ENST00000566069.6:c.109_211del
ENST00000567003.1:n.387_489del
ENST00000568219.5:c.-777_-675del
ENST00000697374.1:c.-777_-675del
ENST00000697375.1:n.1456_1558del
ENST00000697376.1:c.-777_-675del	ENSP00000513285.1:n.-777_-675del
ENST00000697377.1:c.-777_-675del
ENST00000697377.2:c.115_217del
ENST00000697378.1:n.629_731del
ENST00000697379.1:c.-777_-675del
ENST00000697379.2:c.115_217del
ENST00000697382.1:c.-777_-675del
ENST00000697383.1:c.48+3158_48+3260del	ENSP00000513289.1:n.48+3158_48+3260del
ENST00000697384.1:n.263_365del
XM_011545946.1:c.115_217del
XM_011545946.2:c.115_217del
XM_011545947.1:c.115_217del
XM_011545947.2:c.115_217del
XM_011545948.1:c.-777_-675del
XM_011545948.2:c.-777_-675del
XM_017023671.1:c.115_217del
XM_017023672.2:c.109_211del
XM_017023673.2:c.109_211del
XR_950851.1:n.905_1007del