Canonical Allele Identifier: CA916081825

Gene: PALB2

Linked Data

• ClinVar Variation Id: 853702
• ClinVar RCV Id: RCV001058567

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629003_23635190del , CM000678.2:g.23629003_23635190del	GRCh38
NC_000016.9:g.23640324_23646511del , CM000678.1:g.23640324_23646511del	GRCh37
NC_000016.8:g.23547825_23554012del	NCBI36
NG_007406.1:g.11168_17355del , LRG_308:g.11168_17355del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1362_2592+201del
ENST00000565038.2:c.211+2660_*67+201del
ENST00000566069.6:c.1356_2586+201del
ENST00000697377.2:c.1362_2592+201del
ENST00000697379.2:c.1362_2592+201del
ENST00000561514.2:c.471_1701+201del
ENST00000697374.1:c.471_1701+201del
ENST00000697375.1:n.2703_3933+201del
ENST00000697376.1:c.471_1701+201del
ENST00000697377.1:c.471_1701+201del
ENST00000697378.1:n.1876_3106+201del
ENST00000697379.1:c.471_1701+201del
ENST00000697382.1:c.471_1701+201del
ENST00000697383.1:c.49-5915_120+201del
ENST00000261584.9:c.1356_2586+201del
ENST00000261584.8:c.1356_2586+201del
ENST00000565038.1:c.86+2660_158+201del
ENST00000568219.5:c.471_1701+201del
NM_024675.3:c.1356_2586+201del , LRG_308t1:c.1356_2586+201del
XM_011545946.1:c.1362_2592+201del
XM_011545947.1:c.1362_2592+201del
XM_011545948.1:c.471_1701+201del
XR_950851.1:n.2152_3382+201del
XM_011545946.2:c.1362_2592+201del
XM_011545947.2:c.1362_2592+201del
XM_011545948.2:c.471_1701+201del
XM_017023671.1:c.1362_2592+201del
XM_017023672.2:c.1356_2586+201del
XM_017023673.2:c.1356_2586+201del
NM_024675.4:c.1356_2586+201del