Canonical Allele Identifier: CA2632326558
Gene: PALB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621564_23621599del , CM000678.2:g.23621564_23621599del GRCh38
NC_000016.9:g.23632885_23632920del , CM000678.1:g.23632885_23632920del GRCh37
NC_000016.8:g.23540386_23540421del NCBI36
NG_007406.1:g.24762_24797del , LRG_308:g.24762_24797del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3003-118_3003-83del ENSP00000460666.3:n.3003-118_3003-83del
ENST00000565038.2:c.*478-118_*478-83del ENSP00000459882.2:n.*478-118_*478-83del
ENST00000566069.6:c.2997-118_2997-83del ENSP00000459237.2:n.2997-118_2997-83del
ENST00000697377.2:c.2841-118_2841-83del ENSP00000513286.2:n.2841-118_2841-83del
ENST00000697379.2:c.3003-118_3003-83del ENSP00000513287.2:n.3003-118_3003-83del
ENST00000561514.2:c.2112-118_2112-83del ENSP00000460666.2:n.2112-118_2112-83del
ENST00000697374.1:c.2112-118_2112-83del ENSP00000513284.1:n.2112-118_2112-83del
ENST00000697375.1:n.4344-118_4344-83del
ENST00000697376.1:c.2112-118_2112-83del ENSP00000513285.1:n.2112-118_2112-83del
ENST00000697377.1:c.1950-118_1950-83del ENSP00000513286.1:n.1950-118_1950-83del
ENST00000697378.1:n.3517-118_3517-83del
ENST00000697379.1:c.2112-118_2112-83del ENSP00000513287.1:n.2112-118_2112-83del
ENST00000697380.1:n.2289-118_2289-83del
ENST00000697381.1:n.1692-118_1692-83del
ENST00000697382.1:c.2112-118_2112-83del ENSP00000513288.1:n.2112-118_2112-83del
ENST00000697383.1:c.531-118_531-83del ENSP00000513289.1:n.531-118_531-83del
ENST00000261584.9:c.2997-118_2997-83del MANE Select ENSP00000261584.4:n.2997-118_2997-83del
ENST00000261584.8:c.2997-118_2997-83del ENSP00000261584.4:n.2997-118_2997-83del
ENST00000568219.5:c.2112-118_2112-83del ENSP00000454703.2:n.2112-118_2112-83del
NM_024675.3:c.2997-118_2997-83del , LRG_308t1:c.2997-118_2997-83del NP_078951.2:n.2997-118_2997-83del
XM_011545946.1:c.3003-118_3003-83del XP_011544248.1:n.3003-118_3003-83del
XM_011545947.1:c.3003-118_3003-83del XP_011544249.1:n.3003-118_3003-83del
XM_011545948.1:c.2112-118_2112-83del XP_011544250.1:n.2112-118_2112-83del
XR_950851.1:n.3793-118_3793-83del
XM_011545946.2:c.3003-118_3003-83del XP_011544248.1:n.3003-118_3003-83del
XM_011545947.2:c.3003-118_3003-83del XP_011544249.1:n.3003-118_3003-83del
XM_011545948.2:c.2112-118_2112-83del XP_011544250.1:n.2112-118_2112-83del
XM_017023671.1:c.3003-118_3003-83del XP_016879160.1:n.3003-118_3003-83del
XM_017023672.2:c.2997-118_2997-83del XP_016879161.1:n.2997-118_2997-83del
XM_017023673.2:c.2997-118_2997-83del XP_016879162.1:n.2997-118_2997-83del
NM_024675.4:c.2997-118_2997-83del MANE Select NP_078951.2:n.2997-118_2997-83del