Canonical Allele Identifier: CA331794
Gene: PALB2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 126644
dbSNP Id: rs180177084

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23636317del , CM000678.2:g.23636317del GRCh38
NC_000016.9:g.23647638del , CM000678.1:g.23647638del GRCh37
NC_000016.8:g.23555139del NCBI36
NG_007406.1:g.10041del , LRG_308:g.10041del

Transcript Alleles

HGVS Amino-acid change
NM_024675.3:c.229del , LRG_308t1:c.229del NP_078951.2:p.Cys77ValfsTer?
XM_011545946.1:c.235del XP_011544248.1:p.Cys79ValfsTer?
XM_011545947.1:c.235del XP_011544249.1:p.Cys79ValfsTer?
XM_011545948.1:c.-657del XP_011544250.1:p.=
XR_950851.1:n.1025del
XM_011545946.2:c.235del XP_011544248.1:p.Cys79ValfsTer?
XM_011545947.2:c.235del XP_011544249.1:p.Cys79ValfsTer?
XM_011545948.2:c.-657del XP_011544250.1:p.=
XM_017023671.1:c.235del XP_016879160.1:p.Cys79ValfsTer?
XM_017023672.2:c.229del XP_016879161.1:p.Cys77ValfsTer?
XM_017023673.2:c.229del XP_016879162.1:p.Cys77ValfsTer?
ENST00000261584.8:c.229del ENSP00000261584.4:p.Cys77ValfsTer?
ENST00000561514.1:c.235del ENSP00000460666.1:p.Cys79ValfsTer?
ENST00000565038.1:n.86+1533del
ENST00000567003.1:n.507del
ENST00000568219.5:c.-657del ENSP00000454703.2:p.=