Canonical Allele Identifier: CA395138772
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs2142446217

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23636230A>G , CM000678.2:g.23636230A>G GRCh38
NC_000016.9:g.23647551A>G , CM000678.1:g.23647551A>G GRCh37
NC_000016.8:g.23555052A>G NCBI36
NG_007406.1:g.10128T>C , LRG_308:g.10128T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.322T>C ENSP00000460666.3:p.Ser108Pro
ENST00000565038.2:c.211+1620T>C ENSP00000459882.2:n.211+1620T>C
ENST00000566069.6:c.316T>C ENSP00000459237.2:p.Ser106Pro
ENST00000697377.2:c.322T>C ENSP00000513286.2:p.Ser108Pro
ENST00000697379.2:c.322T>C ENSP00000513287.2:p.Ser108Pro
ENST00000561514.2:c.-570T>C ENSP00000460666.2:n.-570T>C
ENST00000697374.1:c.-570T>C ENSP00000513284.1:n.-570T>C
ENST00000697375.1:n.1663T>C
ENST00000697376.1:c.-570T>C ENSP00000513285.1:n.-570T>C
ENST00000697377.1:c.-570T>C ENSP00000513286.1:n.-570T>C
ENST00000697378.1:n.836T>C
ENST00000697379.1:c.-570T>C ENSP00000513287.1:n.-570T>C
ENST00000697382.1:c.-570T>C ENSP00000513288.1:n.-570T>C
ENST00000697383.1:c.48+4880T>C ENSP00000513289.1:n.48+4880T>C
ENST00000697384.1:n.470T>C
ENST00000261584.9:c.316T>C MANE Select ENSP00000261584.4:p.Ser106Pro
ENST00000261584.8:c.316T>C ENSP00000261584.4:p.Ser106Pro
ENST00000565038.1:c.86+1620T>C
ENST00000567003.1:n.594T>C
ENST00000568219.5:c.-570T>C ENSP00000454703.2:n.-570T>C
NM_024675.3:c.316T>C , LRG_308t1:c.316T>C NP_078951.2:p.Ser106Pro
XM_011545946.1:c.322T>C XP_011544248.1:p.Ser108Pro
XM_011545947.1:c.322T>C XP_011544249.1:p.Ser108Pro
XM_011545948.1:c.-570T>C XP_011544250.1:n.-570T>C
XR_950851.1:n.1112T>C
XM_011545946.2:c.322T>C XP_011544248.1:p.Ser108Pro
XM_011545947.2:c.322T>C XP_011544249.1:p.Ser108Pro
XM_011545948.2:c.-570T>C XP_011544250.1:n.-570T>C
XM_017023671.1:c.322T>C XP_016879160.1:p.Ser108Pro
XM_017023672.2:c.316T>C XP_016879161.1:p.Ser106Pro
XM_017023673.2:c.316T>C XP_016879162.1:p.Ser106Pro
NM_024675.4:c.316T>C MANE Select NP_078951.2:p.Ser106Pro