Canonical Allele Identifier: CA2632328359

Gene: PALB2

Linked Data

• gnomAD v4: 16-23637823-A-AGG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23637824_23637825dup , CM000678.2:g.23637824_23637825dup	GRCh38
NC_000016.9:g.23649145_23649146dup , CM000678.1:g.23649145_23649146dup	GRCh37
NC_000016.8:g.23556646_23556647dup	NCBI36
NG_007406.1:g.8533_8534dup , LRG_308:g.8533_8534dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.217+25_217+26dup	ENSP00000460666.3:n.217+25_217+26dup
ENST00000565038.2:c.211+25_211+26dup	ENSP00000459882.2:n.211+25_211+26dup
ENST00000566069.6:c.211+25_211+26dup	ENSP00000459237.2:n.211+25_211+26dup
ENST00000697377.2:c.217+25_217+26dup	ENSP00000513286.2:n.217+25_217+26dup
ENST00000697379.2:c.217+25_217+26dup	ENSP00000513287.2:n.217+25_217+26dup
ENST00000561514.2:c.-675+25_-675+26dup	ENSP00000460666.2:n.-675+25_-675+26dup
ENST00000697374.1:c.-675+25_-675+26dup	ENSP00000513284.1:n.-675+25_-675+26dup
ENST00000697375.1:n.1558+25_1558+26dup
ENST00000697376.1:c.-675+25_-675+26dup	ENSP00000513285.1:n.-675+25_-675+26dup
ENST00000697377.1:c.-675+25_-675+26dup	ENSP00000513286.1:n.-675+25_-675+26dup
ENST00000697378.1:n.731+25_731+26dup
ENST00000697379.1:c.-675+25_-675+26dup	ENSP00000513287.1:n.-675+25_-675+26dup
ENST00000697382.1:c.-675+25_-675+26dup	ENSP00000513288.1:n.-675+25_-675+26dup
ENST00000697383.1:c.48+3285_48+3286dup	ENSP00000513289.1:n.48+3285_48+3286dup
ENST00000697384.1:n.365+25_365+26dup
ENST00000261584.9:c.211+25_211+26dup MANE Select	ENSP00000261584.4:n.211+25_211+26dup
ENST00000261584.8:c.211+25_211+26dup	ENSP00000261584.4:n.211+25_211+26dup
ENST00000561514.1:c.217+25_217+26dup	ENSP00000460666.1:n.217+25_217+26dup
ENST00000565038.1:c.86+25_86+26dup
ENST00000567003.1:n.489+25_489+26dup
ENST00000568219.5:c.-675+25_-675+26dup	ENSP00000454703.2:n.-675+25_-675+26dup
NM_024675.3:c.211+25_211+26dup , LRG_308t1:c.211+25_211+26dup	NP_078951.2:n.211+25_211+26dup
XM_011545946.1:c.217+25_217+26dup	XP_011544248.1:n.217+25_217+26dup
XM_011545947.1:c.217+25_217+26dup	XP_011544249.1:n.217+25_217+26dup
XM_011545948.1:c.-675+25_-675+26dup	XP_011544250.1:n.-675+25_-675+26dup
XR_950851.1:n.1007+25_1007+26dup
XM_011545946.2:c.217+25_217+26dup	XP_011544248.1:n.217+25_217+26dup
XM_011545947.2:c.217+25_217+26dup	XP_011544249.1:n.217+25_217+26dup
XM_011545948.2:c.-675+25_-675+26dup	XP_011544250.1:n.-675+25_-675+26dup
XM_017023671.1:c.217+25_217+26dup	XP_016879160.1:n.217+25_217+26dup
XM_017023672.2:c.211+25_211+26dup	XP_016879161.1:n.211+25_211+26dup
XM_017023673.2:c.211+25_211+26dup	XP_016879162.1:n.211+25_211+26dup
NM_024675.4:c.211+25_211+26dup MANE Select	NP_078951.2:n.211+25_211+26dup