Canonical Allele Identifier: CA395137411
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs2142444314

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23636147A>T , CM000678.2:g.23636147A>T GRCh38
NC_000016.9:g.23647468A>T , CM000678.1:g.23647468A>T GRCh37
NC_000016.8:g.23554969A>T NCBI36
NG_007406.1:g.10211T>A , LRG_308:g.10211T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.405T>A ENSP00000460666.3:p.Ser135Arg
ENST00000565038.2:c.211+1703T>A ENSP00000459882.2:n.211+1703T>A
ENST00000566069.6:c.399T>A ENSP00000459237.2:p.Ser133Arg
ENST00000697377.2:c.405T>A ENSP00000513286.2:p.Ser135Arg
ENST00000697379.2:c.405T>A ENSP00000513287.2:p.Ser135Arg
ENST00000561514.2:c.-487T>A ENSP00000460666.2:n.-487T>A
ENST00000697374.1:c.-487T>A ENSP00000513284.1:n.-487T>A
ENST00000697375.1:n.1746T>A
ENST00000697376.1:c.-487T>A ENSP00000513285.1:n.-487T>A
ENST00000697377.1:c.-487T>A ENSP00000513286.1:n.-487T>A
ENST00000697378.1:n.919T>A
ENST00000697379.1:c.-487T>A ENSP00000513287.1:n.-487T>A
ENST00000697382.1:c.-487T>A ENSP00000513288.1:n.-487T>A
ENST00000697383.1:c.48+4963T>A ENSP00000513289.1:n.48+4963T>A
ENST00000697384.1:n.553T>A
ENST00000261584.9:c.399T>A MANE Select ENSP00000261584.4:p.Ser133Arg
ENST00000261584.8:c.399T>A ENSP00000261584.4:p.Ser133Arg
ENST00000565038.1:c.86+1703T>A
ENST00000567003.1:n.677T>A
ENST00000568219.5:c.-487T>A ENSP00000454703.2:n.-487T>A
NM_024675.3:c.399T>A , LRG_308t1:c.399T>A NP_078951.2:p.Ser133Arg
XM_011545946.1:c.405T>A XP_011544248.1:p.Ser135Arg
XM_011545947.1:c.405T>A XP_011544249.1:p.Ser135Arg
XM_011545948.1:c.-487T>A XP_011544250.1:n.-487T>A
XR_950851.1:n.1195T>A
XM_011545946.2:c.405T>A XP_011544248.1:p.Ser135Arg
XM_011545947.2:c.405T>A XP_011544249.1:p.Ser135Arg
XM_011545948.2:c.-487T>A XP_011544250.1:n.-487T>A
XM_017023671.1:c.405T>A XP_016879160.1:p.Ser135Arg
XM_017023672.2:c.399T>A XP_016879161.1:p.Ser133Arg
XM_017023673.2:c.399T>A XP_016879162.1:p.Ser133Arg
NM_024675.4:c.399T>A MANE Select NP_078951.2:p.Ser133Arg