Canonical Allele Identifier: CA169811
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142935
dbSNP Id: rs587782831

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23636254T>C , CM000678.2:g.23636254T>C GRCh38
NC_000016.9:g.23647575T>C , CM000678.1:g.23647575T>C GRCh37
NC_000016.8:g.23555076T>C NCBI36
NG_007406.1:g.10104A>G , LRG_308:g.10104A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.298A>G ENSP00000460666.3:p.Ile100Val
ENST00000565038.2:c.211+1596A>G ENSP00000459882.2:n.211+1596A>G
ENST00000566069.6:c.292A>G ENSP00000459237.2:p.Ile98Val
ENST00000697377.2:c.298A>G ENSP00000513286.2:p.Ile100Val
ENST00000697379.2:c.298A>G ENSP00000513287.2:p.Ile100Val
ENST00000561514.2:c.-594A>G ENSP00000460666.2:n.-594A>G
ENST00000697374.1:c.-594A>G ENSP00000513284.1:n.-594A>G
ENST00000697375.1:n.1639A>G
ENST00000697376.1:c.-594A>G ENSP00000513285.1:n.-594A>G
ENST00000697377.1:c.-594A>G ENSP00000513286.1:n.-594A>G
ENST00000697378.1:n.812A>G
ENST00000697379.1:c.-594A>G ENSP00000513287.1:n.-594A>G
ENST00000697382.1:c.-594A>G ENSP00000513288.1:n.-594A>G
ENST00000697383.1:c.48+4856A>G ENSP00000513289.1:n.48+4856A>G
ENST00000697384.1:n.446A>G
ENST00000261584.9:c.292A>G MANE Select ENSP00000261584.4:p.Ile98Val
ENST00000261584.8:c.292A>G ENSP00000261584.4:p.Ile98Val
ENST00000565038.1:c.86+1596A>G
ENST00000567003.1:n.570A>G
ENST00000568219.5:c.-594A>G ENSP00000454703.2:n.-594A>G
NM_024675.3:c.292A>G , LRG_308t1:c.292A>G NP_078951.2:p.Ile98Val
XM_011545946.1:c.298A>G XP_011544248.1:p.Ile100Val
XM_011545947.1:c.298A>G XP_011544249.1:p.Ile100Val
XM_011545948.1:c.-594A>G XP_011544250.1:n.-594A>G
XR_950851.1:n.1088A>G
XM_011545946.2:c.298A>G XP_011544248.1:p.Ile100Val
XM_011545947.2:c.298A>G XP_011544249.1:p.Ile100Val
XM_011545948.2:c.-594A>G XP_011544250.1:n.-594A>G
XM_017023671.1:c.298A>G XP_016879160.1:p.Ile100Val
XM_017023672.2:c.292A>G XP_016879161.1:p.Ile98Val
XM_017023673.2:c.292A>G XP_016879162.1:p.Ile98Val
NM_024675.4:c.292A>G MANE Select NP_078951.2:p.Ile98Val