Canonical Allele Identifier: CA395124095
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791691
ClinVar RCV Id: RCV002450582
dbSNP Id: rs1157451265

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23629688C>G , CM000678.2:g.23629688C>G GRCh38
NC_000016.9:g.23641009C>G , CM000678.1:g.23641009C>G GRCh37
NC_000016.8:g.23548510C>G NCBI36
NG_007406.1:g.16670G>C , LRG_308:g.16670G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.2472G>C ENSP00000460666.3:p.Gln824His
ENST00000565038.2:c.212-413G>C ENSP00000459882.2:n.212-413G>C
ENST00000566069.6:c.2466G>C ENSP00000459237.2:p.Gln822His
ENST00000697377.2:c.2472G>C ENSP00000513286.2:p.Gln824His
ENST00000697379.2:c.2472G>C ENSP00000513287.2:p.Gln824His
ENST00000561514.2:c.1581G>C ENSP00000460666.2:p.Gln527His
ENST00000697374.1:c.1581G>C ENSP00000513284.1:p.Gln527His
ENST00000697375.1:n.3813G>C
ENST00000697376.1:c.1581G>C ENSP00000513285.1:p.Gln527His
ENST00000697377.1:c.1581G>C ENSP00000513286.1:p.Gln527His
ENST00000697378.1:n.2986G>C
ENST00000697379.1:c.1581G>C ENSP00000513287.1:p.Gln527His
ENST00000697380.1:n.1394G>C
ENST00000697381.1:n.1161G>C
ENST00000697382.1:c.1581G>C ENSP00000513288.1:p.Gln527His
ENST00000697383.1:c.49-413G>C ENSP00000513289.1:n.49-413G>C
ENST00000697384.1:n.2620G>C
ENST00000261584.9:c.2466G>C MANE Select ENSP00000261584.4:p.Gln822His
ENST00000261584.8:c.2466G>C ENSP00000261584.4:p.Gln822His
ENST00000565038.1:c.87-413G>C
ENST00000568219.5:c.1581G>C ENSP00000454703.2:p.Gln527His
NM_024675.3:c.2466G>C , LRG_308t1:c.2466G>C NP_078951.2:p.Gln822His
XM_011545946.1:c.2472G>C XP_011544248.1:p.Gln824His
XM_011545947.1:c.2472G>C XP_011544249.1:p.Gln824His
XM_011545948.1:c.1581G>C XP_011544250.1:p.Gln527His
XR_950851.1:n.3262G>C
XM_011545946.2:c.2472G>C XP_011544248.1:p.Gln824His
XM_011545947.2:c.2472G>C XP_011544249.1:p.Gln824His
XM_011545948.2:c.1581G>C XP_011544250.1:p.Gln527His
XM_017023671.1:c.2472G>C XP_016879160.1:p.Gln824His
XM_017023672.2:c.2466G>C XP_016879161.1:p.Gln822His
XM_017023673.2:c.2466G>C XP_016879162.1:p.Gln822His
NM_024675.4:c.2466G>C MANE Select NP_078951.2:p.Gln822His