Canonical Allele Identifier: CA3054202301
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23622931_23622991dup , CM000678.2:g.23622931_23622991dup GRCh38
NC_000016.9:g.23634252_23634312dup , CM000678.1:g.23634252_23634312dup GRCh37
NC_000016.8:g.23541753_23541813dup NCBI36
NG_007406.1:g.23368_23428dup , LRG_308:g.23368_23428dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.2981_3002+39dup
ENST00000565038.2:c.*456_*477+39dup
ENST00000566069.6:c.2975_2996+39dup
ENST00000697377.2:c.2819_2840+39dup
ENST00000697379.2:c.2981_3002+39dup
ENST00000561514.2:c.2090_2111+39dup
ENST00000697374.1:c.2090_2111+39dup
ENST00000697375.1:n.4322_4343+39dup
ENST00000697376.1:c.2090_2111+39dup
ENST00000697377.1:c.1928_1949+39dup
ENST00000697378.1:n.3495_3516+39dup
ENST00000697379.1:c.2090_2111+39dup
ENST00000697380.1:n.2267_2288+39dup
ENST00000697381.1:n.1670_1691+39dup
ENST00000697382.1:c.2090_2111+39dup
ENST00000697383.1:c.509_530+39dup
ENST00000261584.9:c.2975_2996+39dup
ENST00000261584.8:c.2975_2996+39dup
ENST00000568219.5:c.2090_2111+39dup
NM_024675.3:c.2975_2996+39dup , LRG_308t1:c.2975_2996+39dup
XM_011545946.1:c.2981_3002+39dup
XM_011545947.1:c.2981_3002+39dup
XM_011545948.1:c.2090_2111+39dup
XR_950851.1:n.3771_3792+39dup
XM_011545946.2:c.2981_3002+39dup
XM_011545947.2:c.2981_3002+39dup
XM_011545948.2:c.2090_2111+39dup
XM_017023671.1:c.2981_3002+39dup
XM_017023672.2:c.2975_2996+39dup
XM_017023673.2:c.2975_2996+39dup
NM_024675.4:c.2975_2996+39dup