Canonical Allele Identifier: CA395142978
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs2142326941

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621410A>G , CM000678.2:g.23621410A>G GRCh38
NC_000016.9:g.23632731A>G , CM000678.1:g.23632731A>G GRCh37
NC_000016.8:g.23540232A>G NCBI36
NG_007406.1:g.24948T>C , LRG_308:g.24948T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3071T>C ENSP00000460666.3:p.Met1024Thr
ENST00000565038.2:c.*546T>C ENSP00000459882.2:n.*546T>C
ENST00000566069.6:c.3065T>C ENSP00000459237.2:p.Met1022Thr
ENST00000697377.2:c.2909T>C ENSP00000513286.2:p.Met970Thr
ENST00000697379.2:c.3071T>C ENSP00000513287.2:p.Met1024Thr
ENST00000561514.2:c.2180T>C ENSP00000460666.2:p.Met727Thr
ENST00000697374.1:c.2180T>C ENSP00000513284.1:p.Met727Thr
ENST00000697375.1:n.4412T>C
ENST00000697376.1:c.2180T>C ENSP00000513285.1:p.Met727Thr
ENST00000697377.1:c.2018T>C ENSP00000513286.1:p.Met673Thr
ENST00000697378.1:n.3585T>C
ENST00000697379.1:c.2180T>C ENSP00000513287.1:p.Met727Thr
ENST00000697380.1:n.2357T>C
ENST00000697381.1:n.1760T>C
ENST00000697382.1:c.2180T>C ENSP00000513288.1:p.Met727Thr
ENST00000697383.1:c.599T>C ENSP00000513289.1:p.Met200Thr
ENST00000261584.9:c.3065T>C MANE Select ENSP00000261584.4:p.Met1022Thr
ENST00000261584.8:c.3065T>C ENSP00000261584.4:p.Met1022Thr
ENST00000568219.5:c.2180T>C ENSP00000454703.2:p.Met727Thr
NM_024675.3:c.3065T>C , LRG_308t1:c.3065T>C NP_078951.2:p.Met1022Thr
XM_011545946.1:c.3071T>C XP_011544248.1:p.Met1024Thr
XM_011545947.1:c.3071T>C XP_011544249.1:p.Met1024Thr
XM_011545948.1:c.2180T>C XP_011544250.1:p.Met727Thr
XR_950851.1:n.3861T>C
XM_011545946.2:c.3071T>C XP_011544248.1:p.Met1024Thr
XM_011545947.2:c.3071T>C XP_011544249.1:p.Met1024Thr
XM_011545948.2:c.2180T>C XP_011544250.1:p.Met727Thr
XM_017023671.1:c.3071T>C XP_016879160.1:p.Met1024Thr
XM_017023672.2:c.3065T>C XP_016879161.1:p.Met1022Thr
XM_017023673.2:c.3065T>C XP_016879162.1:p.Met1022Thr
NM_024675.4:c.3065T>C MANE Select NP_078951.2:p.Met1022Thr