Canonical Allele Identifier: CA1139664609
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 944799
ClinVar RCV Id: RCV001215283
dbSNP Id: rs1567204928

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23603479del , CM000678.2:g.23603479del GRCh38
NC_000016.9:g.23614800del , CM000678.1:g.23614800del GRCh37
NC_000016.8:g.23522301del NCBI36
NG_007406.1:g.42881del , LRG_308:g.42881del

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.3549del ENSP00000460666.3:p.Phe1183LeufsTer10
ENST00000565038.2:c.*1028del ENSP00000459882.2:n.*1028del
ENST00000566069.6:c.*178del ENSP00000459237.2:n.*178del
ENST00000697377.2:c.3387del ENSP00000513286.2:p.Phe1129LeufsTer10
ENST00000697379.2:c.3549del ENSP00000513287.2:p.Phe1183LeufsTer10
ENST00000561514.2:c.2658del ENSP00000460666.2:p.Phe886LeufsTer10
ENST00000697374.1:c.2658del ENSP00000513284.1:p.Phe886LeufsTer10
ENST00000697375.1:n.4890del
ENST00000697376.1:c.*178del ENSP00000513285.1:n.*178del
ENST00000697377.1:c.2496del ENSP00000513286.1:p.Phe832LeufsTer10
ENST00000697378.1:n.4063del
ENST00000697379.1:c.2658del ENSP00000513287.1:p.Phe886LeufsTer10
ENST00000697380.1:n.2747del
ENST00000697381.1:n.2238del
ENST00000697382.1:c.*320del ENSP00000513288.1:n.*320del
ENST00000697383.1:c.1077del ENSP00000513289.1:p.Phe359LeufsTer10
ENST00000261584.9:c.3543del MANE Select ENSP00000261584.4:p.Phe1181LeufsTer10
ENST00000261584.8:c.3543del ENSP00000261584.4:p.Phe1181LeufsTer10
ENST00000566069.5:c.309del
ENST00000568219.5:c.2658del ENSP00000454703.2:p.Phe886LeufsTer10
NM_024675.3:c.3543del , LRG_308t1:c.3543del NP_078951.2:p.Phe1181LeufsTer10
XM_011545946.1:c.3549del XP_011544248.1:p.Phe1183LeufsTer10
XM_011545947.1:c.*178del XP_011544249.1:n.*178del
XM_011545948.1:c.2658del XP_011544250.1:p.Phe886LeufsTer10
XR_950851.1:n.4251del
XM_011545946.2:c.3549del XP_011544248.1:p.Phe1183LeufsTer10
XM_011545947.2:c.*178del XP_011544249.1:n.*178del
XM_011545948.2:c.2658del XP_011544250.1:p.Phe886LeufsTer10
XM_017023671.1:c.3312del XP_016879160.1:p.Phe1104LeufsTer10
XM_017023672.2:c.3306del XP_016879161.1:p.Phe1102LeufsTer10
XM_017023673.2:c.*178del XP_016879162.1:n.*178del
NM_024675.4:c.3543del MANE Select NP_078951.2:p.Phe1181LeufsTer10