Canonical Allele Identifier: CA923726279
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23637941_23641153dup , CM000678.2:g.23637941_23641153dup GRCh38
NC_000016.9:g.23649262_23652474dup , CM000678.1:g.23649262_23652474dup GRCh37
NC_000016.8:g.23556763_23559975dup NCBI36
NG_007406.1:g.5205_8417dup , LRG_308:g.5205_8417dup

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.-848_126dup
ENST00000565038.2:c.5_120dup
ENST00000566069.6:c.5_120dup
ENST00000697377.2:c.-235_126dup
ENST00000697379.2:c.-141_126dup
ENST00000561514.2:c.-1739_-766dup
ENST00000697374.1:c.-1330_-766dup
ENST00000697376.1:c.-1051_-766dup
ENST00000697377.1:c.-1126_-766dup
ENST00000697379.1:c.-1032_-766dup
ENST00000697382.1:c.-1790_-766dup
ENST00000697383.1:c.5_48+3169dup
ENST00000697384.1:n.159_274dup
ENST00000261584.9:c.5_120dup
ENST00000261584.8:c.5_120dup
ENST00000567003.1:n.149_398dup
ENST00000568219.5:c.-864_-766dup
NM_024675.3:c.5_120dup , LRG_308t1:c.5_120dup
XM_011545948.1:c.-1015_-766dup
XM_011545946.2:c.-848_126dup
XM_011545947.2:c.-848_126dup
XM_011545948.2:c.-1015_-766dup
XM_017023671.1:c.-848_126dup
XM_017023672.2:c.5_120dup
XM_017023673.2:c.5_120dup
NM_024675.4:c.5_120dup