Canonical Allele Identifier: CA395137600
Gene: PALB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23603464A>G , CM000678.2:g.23603464A>G GRCh38
NC_000016.9:g.23614785A>G , CM000678.1:g.23614785A>G GRCh37
NC_000016.8:g.23522286A>G NCBI36
NG_007406.1:g.42894T>C , LRG_308:g.42894T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3562T>C ENSP00000460666.3:p.Ser1188Pro
ENST00000565038.2:c.*1041T>C ENSP00000459882.2:n.*1041T>C
ENST00000566069.6:c.*191T>C ENSP00000459237.2:n.*191T>C
ENST00000697377.2:c.3400T>C ENSP00000513286.2:p.Ser1134Pro
ENST00000697379.2:c.3562T>C ENSP00000513287.2:p.Ser1188Pro
ENST00000561514.2:c.2671T>C ENSP00000460666.2:p.Ser891Pro
ENST00000697374.1:c.2671T>C ENSP00000513284.1:p.Ser891Pro
ENST00000697375.1:n.4903T>C
ENST00000697376.1:c.*191T>C ENSP00000513285.1:n.*191T>C
ENST00000697377.1:c.2509T>C ENSP00000513286.1:p.Ser837Pro
ENST00000697378.1:n.4076T>C
ENST00000697379.1:c.2671T>C ENSP00000513287.1:p.Ser891Pro
ENST00000697380.1:n.2760T>C
ENST00000697381.1:n.2251T>C
ENST00000697382.1:c.*333T>C ENSP00000513288.1:n.*333T>C
ENST00000697383.1:c.1090T>C ENSP00000513289.1:p.Ser364Pro
ENST00000261584.9:c.3556T>C MANE Select ENSP00000261584.4:p.Ser1186Pro
ENST00000261584.8:c.3556T>C ENSP00000261584.4:p.Ser1186Pro
ENST00000566069.5:c.322T>C
ENST00000568219.5:c.2671T>C ENSP00000454703.2:p.Ser891Pro
NM_024675.3:c.3556T>C , LRG_308t1:c.3556T>C NP_078951.2:p.Ser1186Pro
XM_011545946.1:c.3562T>C XP_011544248.1:p.Ser1188Pro
XM_011545947.1:c.*191T>C XP_011544249.1:n.*191T>C
XM_011545948.1:c.2671T>C XP_011544250.1:p.Ser891Pro
XR_950851.1:n.4264T>C
XM_011545946.2:c.3562T>C XP_011544248.1:p.Ser1188Pro
XM_011545947.2:c.*191T>C XP_011544249.1:n.*191T>C
XM_011545948.2:c.2671T>C XP_011544250.1:p.Ser891Pro
XM_017023671.1:c.3325T>C XP_016879160.1:p.Ser1109Pro
XM_017023672.2:c.3319T>C XP_016879161.1:p.Ser1107Pro
XM_017023673.2:c.*191T>C XP_016879162.1:n.*191T>C
NM_024675.4:c.3556T>C MANE Select NP_078951.2:p.Ser1186Pro