Canonical Allele Identifier: CA916081810
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23620004_23623427del , CM000678.2:g.23620004_23623427del GRCh38
NC_000016.9:g.23631325_23634748del , CM000678.1:g.23631325_23634748del GRCh37
NC_000016.8:g.23538826_23542249del NCBI36
NG_007406.1:g.22947_26370del , LRG_308:g.22947_26370del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.2841-281_3119+1374del
ENST00000565038.2:c.*316-281_*594+1374del
ENST00000566069.6:c.2835-281_3113+1374del
ENST00000697377.2:c.2679-281_2957+1374del
ENST00000697379.2:c.2841-281_3119+1374del
ENST00000561514.2:c.1950-281_2228+1374del
ENST00000697374.1:c.1950-281_2228+1374del
ENST00000697375.1:n.4182-281_4460+1374del
ENST00000697376.1:c.1950-281_2228+1374del
ENST00000697377.1:c.1788-281_2066+1374del
ENST00000697378.1:n.3355-281_3633+1374del
ENST00000697379.1:c.1950-281_2228+1374del
ENST00000697380.1:n.2127-281_2405+1374del
ENST00000697381.1:n.1530-281_1808+1374del
ENST00000697382.1:c.1950-281_2228+1374del
ENST00000697383.1:c.369-281_647+1374del
ENST00000261584.9:c.2835-281_3113+1374del
ENST00000261584.8:c.2835-281_3113+1374del
ENST00000568219.5:c.1950-281_2228+1374del
NM_024675.3:c.2835-281_3113+1374del , LRG_308t1:c.2835-281_3113+1374del
XM_011545946.1:c.2841-281_3119+1374del
XM_011545947.1:c.2841-281_3119+1374del
XM_011545948.1:c.1950-281_2228+1374del
XR_950851.1:n.3631-281_3909+1374del
XM_011545946.2:c.2841-281_3119+1374del
XM_011545947.2:c.2841-281_3119+1374del
XM_011545948.2:c.1950-281_2228+1374del
XM_017023671.1:c.2841-281_3119+1374del
XM_017023672.2:c.2835-281_3113+1374del
XM_017023673.2:c.2835-281_3113+1374del
NM_024675.4:c.2835-281_3113+1374del