Canonical Allele Identifier: CA2632326606
Gene: PALB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621593_23621596dup , CM000678.2:g.23621593_23621596dup GRCh38
NC_000016.9:g.23632914_23632917dup , CM000678.1:g.23632914_23632917dup GRCh37
NC_000016.8:g.23540415_23540418dup NCBI36
NG_007406.1:g.24762_24765dup , LRG_308:g.24762_24765dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3003-118_3003-115dup ENSP00000460666.3:n.3003-118_3003-115dup
ENST00000565038.2:c.*478-118_*478-115dup ENSP00000459882.2:n.*478-118_*478-115dup
ENST00000566069.6:c.2997-118_2997-115dup ENSP00000459237.2:n.2997-118_2997-115dup
ENST00000697377.2:c.2841-118_2841-115dup ENSP00000513286.2:n.2841-118_2841-115dup
ENST00000697379.2:c.3003-118_3003-115dup ENSP00000513287.2:n.3003-118_3003-115dup
ENST00000561514.2:c.2112-118_2112-115dup ENSP00000460666.2:n.2112-118_2112-115dup
ENST00000697374.1:c.2112-118_2112-115dup ENSP00000513284.1:n.2112-118_2112-115dup
ENST00000697375.1:n.4344-118_4344-115dup
ENST00000697376.1:c.2112-118_2112-115dup ENSP00000513285.1:n.2112-118_2112-115dup
ENST00000697377.1:c.1950-118_1950-115dup ENSP00000513286.1:n.1950-118_1950-115dup
ENST00000697378.1:n.3517-118_3517-115dup
ENST00000697379.1:c.2112-118_2112-115dup ENSP00000513287.1:n.2112-118_2112-115dup
ENST00000697380.1:n.2289-118_2289-115dup
ENST00000697381.1:n.1692-118_1692-115dup
ENST00000697382.1:c.2112-118_2112-115dup ENSP00000513288.1:n.2112-118_2112-115dup
ENST00000697383.1:c.531-118_531-115dup ENSP00000513289.1:n.531-118_531-115dup
ENST00000261584.9:c.2997-118_2997-115dup MANE Select ENSP00000261584.4:n.2997-118_2997-115dup
ENST00000261584.8:c.2997-118_2997-115dup ENSP00000261584.4:n.2997-118_2997-115dup
ENST00000568219.5:c.2112-118_2112-115dup ENSP00000454703.2:n.2112-118_2112-115dup
NM_024675.3:c.2997-118_2997-115dup , LRG_308t1:c.2997-118_2997-115dup NP_078951.2:n.2997-118_2997-115dup
XM_011545946.1:c.3003-118_3003-115dup XP_011544248.1:n.3003-118_3003-115dup
XM_011545947.1:c.3003-118_3003-115dup XP_011544249.1:n.3003-118_3003-115dup
XM_011545948.1:c.2112-118_2112-115dup XP_011544250.1:n.2112-118_2112-115dup
XR_950851.1:n.3793-118_3793-115dup
XM_011545946.2:c.3003-118_3003-115dup XP_011544248.1:n.3003-118_3003-115dup
XM_011545947.2:c.3003-118_3003-115dup XP_011544249.1:n.3003-118_3003-115dup
XM_011545948.2:c.2112-118_2112-115dup XP_011544250.1:n.2112-118_2112-115dup
XM_017023671.1:c.3003-118_3003-115dup XP_016879160.1:n.3003-118_3003-115dup
XM_017023672.2:c.2997-118_2997-115dup XP_016879161.1:n.2997-118_2997-115dup
XM_017023673.2:c.2997-118_2997-115dup XP_016879162.1:n.2997-118_2997-115dup
NM_024675.4:c.2997-118_2997-115dup MANE Select NP_078951.2:n.2997-118_2997-115dup