Canonical Allele Identifier: CA2580061392
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1809518
ClinVar RCV Id: RCV002481097

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621363_23623131del , CM000678.2:g.23621363_23623131del GRCh38
NC_000016.9:g.23632684_23634452del , CM000678.1:g.23632684_23634452del GRCh37
NC_000016.8:g.23540185_23541953del NCBI36
NG_007406.1:g.23229_24997del , LRG_308:g.23229_24997del

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.2842_3119+1del
ENST00000565038.2:c.*317_*594+1del
ENST00000566069.6:c.2836_3113+1del
ENST00000697377.2:c.2680_2957+1del
ENST00000697379.2:c.2842_3119+1del
ENST00000561514.2:c.1951_2228+1del
ENST00000697374.1:c.1951_2228+1del
ENST00000697375.1:n.4183_4460+1del
ENST00000697376.1:c.1951_2228+1del
ENST00000697377.1:c.1789_2066+1del
ENST00000697378.1:n.3356_3633+1del
ENST00000697379.1:c.1951_2228+1del
ENST00000697380.1:n.2128_2405+1del
ENST00000697381.1:n.1531_1808+1del
ENST00000697382.1:c.1951_2228+1del
ENST00000697383.1:c.370_647+1del
ENST00000261584.9:c.2836_3113+1del
ENST00000261584.8:c.2836_3113+1del
ENST00000568219.5:c.1951_2228+1del
NM_024675.3:c.2836_3113+1del , LRG_308t1:c.2836_3113+1del
XM_011545946.1:c.2842_3119+1del
XM_011545947.1:c.2842_3119+1del
XM_011545948.1:c.1951_2228+1del
XR_950851.1:n.3632_3909+1del
XM_011545946.2:c.2842_3119+1del
XM_011545947.2:c.2842_3119+1del
XM_011545948.2:c.1951_2228+1del
XM_017023671.1:c.2842_3119+1del
XM_017023672.2:c.2836_3113+1del
XM_017023673.2:c.2836_3113+1del
NM_024675.4:c.2836_3113+1del