Canonical Allele Identifier: CA294551
Gene: PALB2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 143963
dbSNP Id: rs587776406

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23637905del , CM000678.2:g.23637905del GRCh38
NC_000016.9:g.23649226del , CM000678.1:g.23649226del GRCh37
NC_000016.8:g.23556727del NCBI36
NG_007406.1:g.8453del , LRG_308:g.8453del

Transcript Alleles

HGVS Amino-acid change
NM_024675.3:c.156del , LRG_308t1:c.156del NP_078951.2:p.Glu53LysfsTer15
XM_011545946.1:c.162del XP_011544248.1:p.Glu55LysfsTer15
XM_011545947.1:c.162del XP_011544249.1:p.Glu55LysfsTer15
XM_011545948.1:c.-730del XP_011544250.1:p.=
XR_950851.1:n.952del
XM_011545946.2:c.162del XP_011544248.1:p.Glu55LysfsTer15
XM_011545947.2:c.162del XP_011544249.1:p.Glu55LysfsTer15
XM_011545948.2:c.-730del XP_011544250.1:p.=
XM_017023671.1:c.162del XP_016879160.1:p.Glu55LysfsTer15
XM_017023672.2:c.156del XP_016879161.1:p.Glu53LysfsTer15
XM_017023673.2:c.156del XP_016879162.1:p.Glu53LysfsTer15
ENST00000261584.8:c.156del ENSP00000261584.4:p.Glu53LysfsTer15
ENST00000561514.1:c.162del ENSP00000460666.1:p.Glu55LysfsTer15
ENST00000565038.1:n.31del
ENST00000567003.1:n.434del
ENST00000568219.5:c.-730del ENSP00000454703.2:p.=