Canonical Allele Identifier: CA923726321
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23637946_23641153dup , CM000678.2:g.23637946_23641153dup GRCh38
NC_000016.9:g.23649267_23652474dup , CM000678.1:g.23649267_23652474dup GRCh37
NC_000016.8:g.23556768_23559975dup NCBI36
NG_007406.1:g.5206_8413dup , LRG_308:g.5206_8413dup

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.-847_122dup
ENST00000565038.2:c.6_116dup
ENST00000566069.6:c.6_116dup
ENST00000697377.2:c.-234_122dup
ENST00000697379.2:c.-140_122dup
ENST00000561514.2:c.-1738_-770dup
ENST00000697374.1:c.-1329_-770dup
ENST00000697376.1:c.-1050_-770dup
ENST00000697377.1:c.-1125_-770dup
ENST00000697379.1:c.-1031_-770dup
ENST00000697382.1:c.-1789_-770dup
ENST00000697383.1:c.6_48+3165dup
ENST00000697384.1:n.160_270dup
ENST00000261584.9:c.6_116dup
ENST00000261584.8:c.6_116dup
ENST00000567003.1:n.150_394dup
ENST00000568219.5:c.-863_-770dup
NM_024675.3:c.6_116dup , LRG_308t1:c.6_116dup
XM_011545948.1:c.-1014_-770dup
XM_011545946.2:c.-847_122dup
XM_011545947.2:c.-847_122dup
XM_011545948.2:c.-1014_-770dup
XM_017023671.1:c.-847_122dup
XM_017023672.2:c.6_116dup
XM_017023673.2:c.6_116dup
NM_024675.4:c.6_116dup