Canonical Allele Identifier: CA2695222994

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641131_23641138del , CM000678.2:g.23641131_23641138del	GRCh38
NC_000016.9:g.23652452_23652459del , CM000678.1:g.23652452_23652459del	GRCh37
NC_000016.8:g.23559953_23559960del	NCBI36
NG_007406.1:g.5223_5230del , LRG_308:g.5223_5230del

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.-830_-823del	ENSP00000460666.3:n.-830_-823del
ENST00000565038.2:c.23_30del	ENSP00000459882.2:p.Pro8LeufsTer2
ENST00000566069.6:c.23_30del	ENSP00000459237.2:p.Pro8LeufsTer2
ENST00000697377.2:c.-217_-210del	ENSP00000513286.2:n.-217_-210del
ENST00000697379.2:c.-123_-116del	ENSP00000513287.2:n.-123_-116del
ENST00000561514.2:c.-1721_-1714del	ENSP00000460666.2:n.-1721_-1714del
ENST00000697374.1:c.-1312_-1305del	ENSP00000513284.1:n.-1312_-1305del
ENST00000697376.1:c.-1033_-1026del	ENSP00000513285.1:n.-1033_-1026del
ENST00000697377.1:c.-1108_-1101del	ENSP00000513286.1:n.-1108_-1101del
ENST00000697379.1:c.-1014_-1007del	ENSP00000513287.1:n.-1014_-1007del
ENST00000697382.1:c.-1772_-1765del	ENSP00000513288.1:n.-1772_-1765del
ENST00000697383.1:c.23_30del	ENSP00000513289.1:p.Pro8LeufsTer2
ENST00000697384.1:n.177_184del
ENST00000261584.9:c.23_30del MANE Select	ENSP00000261584.4:p.Pro8LeufsTer2
ENST00000261584.8:c.23_30del	ENSP00000261584.4:p.Pro8LeufsTer2
ENST00000567003.1:n.167_174del
ENST00000568219.5:c.-846_-839del	ENSP00000454703.2:n.-846_-839del
NM_024675.3:c.23_30del , LRG_308t1:c.23_30del	NP_078951.2:p.Pro8LeufsTer2
XM_011545948.1:c.-997_-990del	XP_011544250.1:n.-997_-990del
XM_011545946.2:c.-830_-823del	XP_011544248.1:n.-830_-823del
XM_011545947.2:c.-830_-823del	XP_011544249.1:n.-830_-823del
XM_011545948.2:c.-997_-990del	XP_011544250.1:n.-997_-990del
XM_017023671.1:c.-830_-823del	XP_016879160.1:n.-830_-823del
XM_017023672.2:c.23_30del	XP_016879161.1:p.Pro8LeufsTer2
XM_017023673.2:c.23_30del	XP_016879162.1:p.Pro8LeufsTer2
NM_024675.4:c.23_30del MANE Select	NP_078951.2:p.Pro8LeufsTer2