Canonical Allele Identifier: CA2632323451

Gene: PALB2

Linked Data

• gnomAD v4: 16-23613983-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23613986del , CM000678.2:g.23613986del	GRCh38
NC_000016.9:g.23625307del , CM000678.1:g.23625307del	GRCh37
NC_000016.8:g.23532808del	NCBI36
NG_007406.1:g.32374del , LRG_308:g.32374del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3207+20del	ENSP00000460666.3:n.3207+20del
ENST00000565038.2:c.*682+20del	ENSP00000459882.2:n.*682+20del
ENST00000566069.6:c.3201+20del	ENSP00000459237.2:n.3201+20del
ENST00000697377.2:c.3045+20del	ENSP00000513286.2:n.3045+20del
ENST00000697379.2:c.3207+20del	ENSP00000513287.2:n.3207+20del
ENST00000561514.2:c.2316+20del	ENSP00000460666.2:n.2316+20del
ENST00000697374.1:c.2316+20del	ENSP00000513284.1:n.2316+20del
ENST00000697375.1:n.4548+20del
ENST00000697376.1:c.2316+20del	ENSP00000513285.1:n.2316+20del
ENST00000697377.1:c.2154+20del	ENSP00000513286.1:n.2154+20del
ENST00000697378.1:n.3721+20del
ENST00000697379.1:c.2316+20del	ENSP00000513287.1:n.2316+20del
ENST00000697380.1:n.2406-5972del
ENST00000697381.1:n.1896+20del
ENST00000697382.1:c.2229-5972del	ENSP00000513288.1:n.2229-5972del
ENST00000697383.1:c.735+20del	ENSP00000513289.1:n.735+20del
ENST00000261584.9:c.3201+20del MANE Select	ENSP00000261584.4:n.3201+20del
ENST00000261584.8:c.3201+20del	ENSP00000261584.4:n.3201+20del
ENST00000566069.5:c.116+20del
ENST00000568219.5:c.2316+20del	ENSP00000454703.2:n.2316+20del
NM_024675.3:c.3201+20del , LRG_308t1:c.3201+20del	NP_078951.2:n.3201+20del
XM_011545946.1:c.3207+20del	XP_011544248.1:n.3207+20del
XM_011545947.1:c.3207+20del	XP_011544249.1:n.3207+20del
XM_011545948.1:c.2316+20del	XP_011544250.1:n.2316+20del
XR_950851.1:n.3910-5972del
XM_011545946.2:c.3207+20del	XP_011544248.1:n.3207+20del
XM_011545947.2:c.3207+20del	XP_011544249.1:n.3207+20del
XM_011545948.2:c.2316+20del	XP_011544250.1:n.2316+20del
XM_017023671.1:c.3119+7378del	XP_016879160.1:n.3119+7378del
XM_017023672.2:c.3113+7378del	XP_016879161.1:n.3113+7378del
XM_017023673.2:c.3201+20del	XP_016879162.1:n.3201+20del
NM_024675.4:c.3201+20del MANE Select	NP_078951.2:n.3201+20del