Canonical Allele Identifier: CA915949163

Gene: PALB2

Linked Data

• ClinVar Variation Id: 659444
• ClinVar RCV Id: RCV000816456
• dbSNP Id: rs1597073423

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23614092del , CM000678.2:g.23614092del	GRCh38
NC_000016.9:g.23625413del , CM000678.1:g.23625413del	GRCh37
NC_000016.8:g.23532914del	NCBI36
NG_007406.1:g.32267del , LRG_308:g.32267del

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3120del
ENST00000565038.2:c.*595del
ENST00000566069.6:c.3114del
ENST00000697377.2:c.2958del
ENST00000697379.2:c.3120del
ENST00000561514.2:c.2229del
ENST00000697374.1:c.2229del
ENST00000697375.1:n.4461del
ENST00000697376.1:c.2229del
ENST00000697377.1:c.2067del
ENST00000697378.1:n.3634del
ENST00000697379.1:c.2229del
ENST00000697380.1:n.2406-6079del
ENST00000697381.1:n.1809del
ENST00000697382.1:c.2229-6079del	ENSP00000513288.1:n.2229-6079del
ENST00000697383.1:c.648del
ENST00000261584.9:c.3114del
ENST00000261584.8:c.3114del
ENST00000566069.5:c.29del
ENST00000568219.5:c.2229del
NM_024675.3:c.3114del , LRG_308t1:c.3114del
XM_011545946.1:c.3120del
XM_011545947.1:c.3120del
XM_011545948.1:c.2229del
XR_950851.1:n.3910-6079del
XM_011545946.2:c.3120del
XM_011545947.2:c.3120del
XM_011545948.2:c.2229del
XM_017023671.1:c.3119+7271del	XP_016879160.1:n.3119+7271del
XM_017023672.2:c.3113+7271del	XP_016879161.1:n.3113+7271del
XM_017023673.2:c.3114del
NM_024675.4:c.3114del