Canonical Allele Identifier: CA395125434
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788638
ClinVar RCV Id: RCV002443747
dbSNP Id: rs1966858206

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23629893G>C , CM000678.2:g.23629893G>C GRCh38
NC_000016.9:g.23641214G>C , CM000678.1:g.23641214G>C GRCh37
NC_000016.8:g.23548715G>C NCBI36
NG_007406.1:g.16465C>G , LRG_308:g.16465C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.2267C>G ENSP00000460666.3:p.Thr756Ser
ENST00000565038.2:c.212-618C>G ENSP00000459882.2:n.212-618C>G
ENST00000566069.6:c.2261C>G ENSP00000459237.2:p.Thr754Ser
ENST00000697377.2:c.2267C>G ENSP00000513286.2:p.Thr756Ser
ENST00000697379.2:c.2267C>G ENSP00000513287.2:p.Thr756Ser
ENST00000561514.2:c.1376C>G ENSP00000460666.2:p.Thr459Ser
ENST00000697374.1:c.1376C>G ENSP00000513284.1:p.Thr459Ser
ENST00000697375.1:n.3608C>G
ENST00000697376.1:c.1376C>G ENSP00000513285.1:p.Thr459Ser
ENST00000697377.1:c.1376C>G ENSP00000513286.1:p.Thr459Ser
ENST00000697378.1:n.2781C>G
ENST00000697379.1:c.1376C>G ENSP00000513287.1:p.Thr459Ser
ENST00000697380.1:n.1189C>G
ENST00000697381.1:n.956C>G
ENST00000697382.1:c.1376C>G ENSP00000513288.1:p.Thr459Ser
ENST00000697383.1:c.49-618C>G ENSP00000513289.1:n.49-618C>G
ENST00000697384.1:n.2415C>G
ENST00000261584.9:c.2261C>G MANE Select ENSP00000261584.4:p.Thr754Ser
ENST00000261584.8:c.2261C>G ENSP00000261584.4:p.Thr754Ser
ENST00000565038.1:c.87-618C>G
ENST00000568219.5:c.1376C>G ENSP00000454703.2:p.Thr459Ser
NM_024675.3:c.2261C>G , LRG_308t1:c.2261C>G NP_078951.2:p.Thr754Ser
XM_011545946.1:c.2267C>G XP_011544248.1:p.Thr756Ser
XM_011545947.1:c.2267C>G XP_011544249.1:p.Thr756Ser
XM_011545948.1:c.1376C>G XP_011544250.1:p.Thr459Ser
XR_950851.1:n.3057C>G
XM_011545946.2:c.2267C>G XP_011544248.1:p.Thr756Ser
XM_011545947.2:c.2267C>G XP_011544249.1:p.Thr756Ser
XM_011545948.2:c.1376C>G XP_011544250.1:p.Thr459Ser
XM_017023671.1:c.2267C>G XP_016879160.1:p.Thr756Ser
XM_017023672.2:c.2261C>G XP_016879161.1:p.Thr754Ser
XM_017023673.2:c.2261C>G XP_016879162.1:p.Thr754Ser
NM_024675.4:c.2261C>G MANE Select NP_078951.2:p.Thr754Ser