Canonical Allele Identifier: CA10588603
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 265584
ClinVar RCV Id: RCV000255792
dbSNP Id: rs886039645

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621433_23621434del , CM000678.2:g.23621433_23621434del GRCh38
NC_000016.9:g.23632754_23632755del , CM000678.1:g.23632754_23632755del GRCh37
NC_000016.8:g.23540255_23540256del NCBI36
NG_007406.1:g.24924_24925del , LRG_308:g.24924_24925del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3047_3048del ENSP00000460666.3:p.Leu1016HisfsTer4
ENST00000565038.2:c.*522_*523del ENSP00000459882.2:n.*522_*523del
ENST00000566069.6:c.3041_3042del ENSP00000459237.2:p.Leu1014HisfsTer4
ENST00000697377.2:c.2885_2886del ENSP00000513286.2:p.Leu962HisfsTer4
ENST00000697379.2:c.3047_3048del ENSP00000513287.2:p.Leu1016HisfsTer4
ENST00000561514.2:c.2156_2157del ENSP00000460666.2:p.Leu719HisfsTer4
ENST00000697374.1:c.2156_2157del ENSP00000513284.1:p.Leu719HisfsTer4
ENST00000697375.1:n.4388_4389del
ENST00000697376.1:c.2156_2157del ENSP00000513285.1:p.Leu719HisfsTer4
ENST00000697377.1:c.1994_1995del ENSP00000513286.1:p.Leu665HisfsTer4
ENST00000697378.1:n.3561_3562del
ENST00000697379.1:c.2156_2157del ENSP00000513287.1:p.Leu719HisfsTer4
ENST00000697380.1:n.2333_2334del
ENST00000697381.1:n.1736_1737del
ENST00000697382.1:c.2156_2157del ENSP00000513288.1:p.Leu719HisfsTer4
ENST00000697383.1:c.575_576del ENSP00000513289.1:p.Leu192HisfsTer4
ENST00000261584.9:c.3041_3042del MANE Select ENSP00000261584.4:p.Leu1014HisfsTer4
ENST00000261584.8:c.3041_3042del ENSP00000261584.4:p.Leu1014HisfsTer4
ENST00000568219.5:c.2156_2157del ENSP00000454703.2:p.Leu719HisfsTer4
NM_024675.3:c.3041_3042del , LRG_308t1:c.3041_3042del NP_078951.2:p.Leu1014HisfsTer4
XM_011545946.1:c.3047_3048del XP_011544248.1:p.Leu1016HisfsTer4
XM_011545947.1:c.3047_3048del XP_011544249.1:p.Leu1016HisfsTer4
XM_011545948.1:c.2156_2157del XP_011544250.1:p.Leu719HisfsTer4
XR_950851.1:n.3837_3838del
XM_011545946.2:c.3047_3048del XP_011544248.1:p.Leu1016HisfsTer4
XM_011545947.2:c.3047_3048del XP_011544249.1:p.Leu1016HisfsTer4
XM_011545948.2:c.2156_2157del XP_011544250.1:p.Leu719HisfsTer4
XM_017023671.1:c.3047_3048del XP_016879160.1:p.Leu1016HisfsTer4
XM_017023672.2:c.3041_3042del XP_016879161.1:p.Leu1014HisfsTer4
XM_017023673.2:c.3041_3042del XP_016879162.1:p.Leu1014HisfsTer4
NM_024675.4:c.3041_3042del MANE Select NP_078951.2:p.Leu1014HisfsTer4