Canonical Allele Identifier: CA395130944
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs2142413433

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23635017C>T , CM000678.2:g.23635017C>T GRCh38
NC_000016.9:g.23646338C>T , CM000678.1:g.23646338C>T GRCh37
NC_000016.8:g.23553839C>T NCBI36
NG_007406.1:g.11341G>A , LRG_308:g.11341G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.1535G>A ENSP00000460666.3:p.Arg512Lys
ENST00000565038.2:c.211+2833G>A ENSP00000459882.2:n.211+2833G>A
ENST00000566069.6:c.1529G>A ENSP00000459237.2:p.Arg510Lys
ENST00000697377.2:c.1535G>A ENSP00000513286.2:p.Arg512Lys
ENST00000697379.2:c.1535G>A ENSP00000513287.2:p.Arg512Lys
ENST00000561514.2:c.644G>A ENSP00000460666.2:p.Arg215Lys
ENST00000697374.1:c.644G>A ENSP00000513284.1:p.Arg215Lys
ENST00000697375.1:n.2876G>A
ENST00000697376.1:c.644G>A ENSP00000513285.1:p.Arg215Lys
ENST00000697377.1:c.644G>A ENSP00000513286.1:p.Arg215Lys
ENST00000697378.1:n.2049G>A
ENST00000697379.1:c.644G>A ENSP00000513287.1:p.Arg215Lys
ENST00000697382.1:c.644G>A ENSP00000513288.1:p.Arg215Lys
ENST00000697383.1:c.49-5742G>A ENSP00000513289.1:n.49-5742G>A
ENST00000697384.1:n.1683G>A
ENST00000261584.9:c.1529G>A MANE Select ENSP00000261584.4:p.Arg510Lys
ENST00000261584.8:c.1529G>A ENSP00000261584.4:p.Arg510Lys
ENST00000565038.1:c.86+2833G>A
ENST00000568219.5:c.644G>A ENSP00000454703.2:p.Arg215Lys
NM_024675.3:c.1529G>A , LRG_308t1:c.1529G>A NP_078951.2:p.Arg510Lys
XM_011545946.1:c.1535G>A XP_011544248.1:p.Arg512Lys
XM_011545947.1:c.1535G>A XP_011544249.1:p.Arg512Lys
XM_011545948.1:c.644G>A XP_011544250.1:p.Arg215Lys
XR_950851.1:n.2325G>A
XM_011545946.2:c.1535G>A XP_011544248.1:p.Arg512Lys
XM_011545947.2:c.1535G>A XP_011544249.1:p.Arg512Lys
XM_011545948.2:c.644G>A XP_011544250.1:p.Arg215Lys
XM_017023671.1:c.1535G>A XP_016879160.1:p.Arg512Lys
XM_017023672.2:c.1529G>A XP_016879161.1:p.Arg510Lys
XM_017023673.2:c.1529G>A XP_016879162.1:p.Arg510Lys
NM_024675.4:c.1529G>A MANE Select NP_078951.2:p.Arg510Lys