Canonical Allele Identifier: CA196834
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 187141
dbSNP Id: rs749494645

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23635167T>C , CM000678.2:g.23635167T>C GRCh38
NC_000016.9:g.23646488T>C , CM000678.1:g.23646488T>C GRCh37
NC_000016.8:g.23553989T>C NCBI36
NG_007406.1:g.11191A>G , LRG_308:g.11191A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.1385A>G ENSP00000460666.3:p.Gln462Arg
ENST00000565038.2:c.211+2683A>G ENSP00000459882.2:n.211+2683A>G
ENST00000566069.6:c.1379A>G ENSP00000459237.2:p.Gln460Arg
ENST00000697377.2:c.1385A>G ENSP00000513286.2:p.Gln462Arg
ENST00000697379.2:c.1385A>G ENSP00000513287.2:p.Gln462Arg
ENST00000561514.2:c.494A>G ENSP00000460666.2:p.Gln165Arg
ENST00000697374.1:c.494A>G ENSP00000513284.1:p.Gln165Arg
ENST00000697375.1:n.2726A>G
ENST00000697376.1:c.494A>G ENSP00000513285.1:p.Gln165Arg
ENST00000697377.1:c.494A>G ENSP00000513286.1:p.Gln165Arg
ENST00000697378.1:n.1899A>G
ENST00000697379.1:c.494A>G ENSP00000513287.1:p.Gln165Arg
ENST00000697382.1:c.494A>G ENSP00000513288.1:p.Gln165Arg
ENST00000697383.1:c.49-5892A>G ENSP00000513289.1:n.49-5892A>G
ENST00000697384.1:n.1533A>G
ENST00000261584.9:c.1379A>G MANE Select ENSP00000261584.4:p.Gln460Arg
ENST00000261584.8:c.1379A>G ENSP00000261584.4:p.Gln460Arg
ENST00000565038.1:c.86+2683A>G
ENST00000568219.5:c.494A>G ENSP00000454703.2:p.Gln165Arg
NM_024675.3:c.1379A>G , LRG_308t1:c.1379A>G NP_078951.2:p.Gln460Arg
XM_011545946.1:c.1385A>G XP_011544248.1:p.Gln462Arg
XM_011545947.1:c.1385A>G XP_011544249.1:p.Gln462Arg
XM_011545948.1:c.494A>G XP_011544250.1:p.Gln165Arg
XR_950851.1:n.2175A>G
XM_011545946.2:c.1385A>G XP_011544248.1:p.Gln462Arg
XM_011545947.2:c.1385A>G XP_011544249.1:p.Gln462Arg
XM_011545948.2:c.494A>G XP_011544250.1:p.Gln165Arg
XM_017023671.1:c.1385A>G XP_016879160.1:p.Gln462Arg
XM_017023672.2:c.1379A>G XP_016879161.1:p.Gln460Arg
XM_017023673.2:c.1379A>G XP_016879162.1:p.Gln460Arg
NM_024675.4:c.1379A>G MANE Select NP_078951.2:p.Gln460Arg