Canonical Allele Identifier: CA279501900

Gene: PALB2

Linked Data

• ClinVar Variation Id: 449888
• ClinVar RCV Id: RCV000523351 ; RCV001063588 ; RCV003446134 ; RCV000774647
• dbSNP Id: rs573118236
• gnomAD v2: 16-23649263-C-T
• gnomAD v3: 16-23637942-C-T
• gnomAD v4: 16-23637942-C-T
• MyVariant Identifiers: chr16:g.23649263C>T (hg19) ; chr16:g.23637942C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23637942C>T , CM000678.2:g.23637942C>T	GRCh38
NC_000016.9:g.23649263C>T , CM000678.1:g.23649263C>T	GRCh37
NC_000016.8:g.23556764C>T	NCBI36
NG_007406.1:g.8416G>A , LRG_308:g.8416G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.125G>A	ENSP00000460666.3:p.Arg42Lys
ENST00000565038.2:c.119G>A	ENSP00000459882.2:p.Arg40Lys
ENST00000566069.6:c.119G>A	ENSP00000459237.2:p.Arg40Lys
ENST00000697377.2:c.125G>A	ENSP00000513286.2:p.Arg42Lys
ENST00000697379.2:c.125G>A	ENSP00000513287.2:p.Arg42Lys
ENST00000561514.2:c.-767G>A	ENSP00000460666.2:n.-767G>A
ENST00000697374.1:c.-767G>A	ENSP00000513284.1:n.-767G>A
ENST00000697375.1:n.1466G>A
ENST00000697376.1:c.-767G>A	ENSP00000513285.1:n.-767G>A
ENST00000697377.1:c.-767G>A	ENSP00000513286.1:n.-767G>A
ENST00000697378.1:n.639G>A
ENST00000697379.1:c.-767G>A	ENSP00000513287.1:n.-767G>A
ENST00000697382.1:c.-767G>A	ENSP00000513288.1:n.-767G>A
ENST00000697383.1:c.48+3168G>A	ENSP00000513289.1:n.48+3168G>A
ENST00000697384.1:n.273G>A
ENST00000261584.9:c.119G>A MANE Select	ENSP00000261584.4:p.Arg40Lys
ENST00000261584.8:c.119G>A	ENSP00000261584.4:p.Arg40Lys
ENST00000561514.1:c.125G>A	ENSP00000460666.1:p.Arg42Lys
ENST00000567003.1:n.397G>A
ENST00000568219.5:c.-767G>A	ENSP00000454703.2:n.-767G>A
NM_024675.3:c.119G>A , LRG_308t1:c.119G>A	NP_078951.2:p.Arg40Lys
XM_011545946.1:c.125G>A	XP_011544248.1:p.Arg42Lys
XM_011545947.1:c.125G>A	XP_011544249.1:p.Arg42Lys
XM_011545948.1:c.-767G>A	XP_011544250.1:n.-767G>A
XR_950851.1:n.915G>A
XM_011545946.2:c.125G>A	XP_011544248.1:p.Arg42Lys
XM_011545947.2:c.125G>A	XP_011544249.1:p.Arg42Lys
XM_011545948.2:c.-767G>A	XP_011544250.1:n.-767G>A
XM_017023671.1:c.125G>A	XP_016879160.1:p.Arg42Lys
XM_017023672.2:c.119G>A	XP_016879161.1:p.Arg40Lys
XM_017023673.2:c.119G>A	XP_016879162.1:p.Arg40Lys
NM_024675.4:c.119G>A MANE Select	NP_078951.2:p.Arg40Lys