Canonical Allele Identifier: CA2580091269

Gene: PALB2

Linked Data

• ClinVar Variation Id: 2089716
• ClinVar RCV Id: RCV003020548
• gnomAD v4: 16-23607907-C-CGCTGA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23607909_23607913dup , CM000678.2:g.23607909_23607913dup	GRCh38
NC_000016.9:g.23619230_23619234dup , CM000678.1:g.23619230_23619234dup	GRCh37
NC_000016.8:g.23526731_23526735dup	NCBI36
NG_007406.1:g.38446_38450dup , LRG_308:g.38446_38450dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3308_3312dup	ENSP00000460666.3:p.Val1105SerfsTer5
ENST00000565038.2:c.*783_*787dup	ENSP00000459882.2:n.*783_*787dup
ENST00000566069.6:c.3202-4243_3202-4239dup	ENSP00000459237.2:n.3202-4243_3202-4239du...
ENST00000697377.2:c.3146_3150dup	ENSP00000513286.2:p.Val1051SerfsTer5
ENST00000697379.2:c.3308_3312dup	ENSP00000513287.2:p.Val1105SerfsTer5
ENST00000561514.2:c.2417_2421dup	ENSP00000460666.2:p.Val808SerfsTer5
ENST00000697374.1:c.2417_2421dup	ENSP00000513284.1:p.Val808SerfsTer5
ENST00000697375.1:n.4649_4653dup
ENST00000697376.1:c.2317-4243_2317-4239dup	ENSP00000513285.1:n.2317-4243_2317-4239du...
ENST00000697377.1:c.2255_2259dup	ENSP00000513286.1:p.Val754SerfsTer5
ENST00000697378.1:n.3822_3826dup
ENST00000697379.1:c.2417_2421dup	ENSP00000513287.1:p.Val808SerfsTer5
ENST00000697380.1:n.2506_2510dup
ENST00000697381.1:n.1997_2001dup
ENST00000697382.1:c.*79_*83dup	ENSP00000513288.1:n.*79_*83dup
ENST00000697383.1:c.836_840dup	ENSP00000513289.1:p.Val281SerfsTer5
ENST00000261584.9:c.3302_3306dup MANE Select	ENSP00000261584.4:p.Val1103SerfsTer5
ENST00000261584.8:c.3302_3306dup	ENSP00000261584.4:p.Val1103SerfsTer5
ENST00000566069.5:c.117-4243_117-4239dup
ENST00000568219.5:c.2417_2421dup	ENSP00000454703.2:p.Val808SerfsTer5
NM_024675.3:c.3302_3306dup , LRG_308t1:c.3302_3306dup	NP_078951.2:p.Val1103SerfsTer5
XM_011545946.1:c.3308_3312dup	XP_011544248.1:p.Val1105SerfsTer5
XM_011545947.1:c.3208-4243_3208-4239dup	XP_011544249.1:n.3208-4243_3208-4239dup
XM_011545948.1:c.2417_2421dup	XP_011544250.1:p.Val808SerfsTer5
XR_950851.1:n.4010_4014dup
XM_011545946.2:c.3308_3312dup	XP_011544248.1:p.Val1105SerfsTer5
XM_011545947.2:c.3208-4243_3208-4239dup	XP_011544249.1:n.3208-4243_3208-4239dup
XM_011545948.2:c.2417_2421dup	XP_011544250.1:p.Val808SerfsTer5
XM_017023671.1:c.3120-4243_3120-4239dup	XP_016879160.1:n.3120-4243_3120-4239dup
XM_017023672.2:c.3114-4243_3114-4239dup	XP_016879161.1:n.3114-4243_3114-4239dup
XM_017023673.2:c.3202-4243_3202-4239dup	XP_016879162.1:n.3202-4243_3202-4239dup
NM_024675.4:c.3302_3306dup MANE Select	NP_078951.2:p.Val1103SerfsTer5