Canonical Allele Identifier: CA3265662811

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23638001_23638080del , CM000678.2:g.23638001_23638080del	GRCh38
NC_000016.9:g.23649322_23649401del , CM000678.1:g.23649322_23649401del	GRCh37
NC_000016.8:g.23556823_23556902del	NCBI36
NG_007406.1:g.8278_8357del , LRG_308:g.8278_8357del

Transcript Alleles

HGVS	Amino-acid Change
NM_024675.3:c.98_109-49del , LRG_308t1:c.98_109-49del
NM_024675.4:c.98_109-49del
ENST00000261584.8:c.98_109-49del
ENST00000261584.9:c.98_109-49del
ENST00000561514.1:c.104_115-49del
ENST00000561514.2:c.-788_-777-49del
ENST00000561514.3:c.104_115-49del
ENST00000565038.2:c.98_109-49del
ENST00000566069.6:c.98_109-49del
ENST00000567003.1:n.376_387-49del
ENST00000568219.5:c.-788_-777-49del
ENST00000697374.1:c.-788_-777-49del
ENST00000697375.1:n.1445_1456-49del
ENST00000697376.1:c.-824_-813-13del
ENST00000697377.1:c.-788_-777-49del
ENST00000697377.2:c.104_115-49del
ENST00000697378.1:n.618_629-49del
ENST00000697379.1:c.-788_-777-49del
ENST00000697379.2:c.104_115-49del
ENST00000697382.1:c.-788_-777-49del
ENST00000697383.1:c.48+3030_48+3109del	ENSP00000513289.1:n.48+3030_48+3109del
ENST00000697384.1:n.252_263-49del
XM_011545946.1:c.104_115-49del
XM_011545946.2:c.104_115-49del
XM_011545947.1:c.104_115-49del
XM_011545947.2:c.104_115-49del
XM_011545948.1:c.-788_-777-49del
XM_011545948.2:c.-788_-777-49del
XM_017023671.1:c.104_115-49del
XM_017023672.2:c.98_109-49del
XM_017023673.2:c.98_109-49del
XR_950851.1:n.894_905-49del