Canonical Allele Identifier: CA2213410549
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621585_23621587delinsGAA , CM000678.2:g.23621585_23621587delinsGAA GRCh38
NC_000016.9:g.23632906_23632908delinsGAA , CM000678.1:g.23632906_23632908delinsGAA GRCh37
NC_000016.8:g.23540407_23540409delinsGAA NCBI36
NG_007406.1:g.24771_24773delinsTTC , LRG_308:g.24771_24773delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3003-109_3003-107delinsTTC ENSP00000460666.3:n.3003-109_3003-107delinsTTC
ENST00000565038.2:c.*478-109_*478-107delinsTTC ENSP00000459882.2:n.*478-109_*478-107delinsTTC
ENST00000566069.6:c.2997-109_2997-107delinsTTC ENSP00000459237.2:n.2997-109_2997-107delinsTTC
ENST00000697377.2:c.2841-109_2841-107delinsTTC ENSP00000513286.2:n.2841-109_2841-107delinsTTC
ENST00000697379.2:c.3003-109_3003-107delinsTTC ENSP00000513287.2:n.3003-109_3003-107delinsTTC
ENST00000561514.2:c.2112-109_2112-107delinsTTC ENSP00000460666.2:n.2112-109_2112-107delinsTTC
ENST00000697374.1:c.2112-109_2112-107delinsTTC ENSP00000513284.1:n.2112-109_2112-107delinsTTC
ENST00000697375.1:n.4344-109_4344-107delinsTTC
ENST00000697376.1:c.2112-109_2112-107delinsTTC ENSP00000513285.1:n.2112-109_2112-107delinsTTC
ENST00000697377.1:c.1950-109_1950-107delinsTTC ENSP00000513286.1:n.1950-109_1950-107delinsTTC
ENST00000697378.1:n.3517-109_3517-107delinsTTC
ENST00000697379.1:c.2112-109_2112-107delinsTTC ENSP00000513287.1:n.2112-109_2112-107delinsTTC
ENST00000697380.1:n.2289-109_2289-107delinsTTC
ENST00000697381.1:n.1692-109_1692-107delinsTTC
ENST00000697382.1:c.2112-109_2112-107delinsTTC ENSP00000513288.1:n.2112-109_2112-107delinsTTC
ENST00000697383.1:c.531-109_531-107delinsTTC ENSP00000513289.1:n.531-109_531-107delinsTTC
ENST00000261584.9:c.2997-109_2997-107delinsTTC MANE Select ENSP00000261584.4:n.2997-109_2997-107delinsTTC
ENST00000261584.8:c.2997-109_2997-107delinsTTC ENSP00000261584.4:n.2997-109_2997-107delinsTTC
ENST00000568219.5:c.2112-109_2112-107delinsTTC ENSP00000454703.2:n.2112-109_2112-107delinsTTC
NM_024675.3:c.2997-109_2997-107delinsTTC , LRG_308t1:c.2997-109_2997-107delinsTTC NP_078951.2:n.2997-109_2997-107delinsTTC
XM_011545946.1:c.3003-109_3003-107delinsTTC XP_011544248.1:n.3003-109_3003-107delinsTTC
XM_011545947.1:c.3003-109_3003-107delinsTTC XP_011544249.1:n.3003-109_3003-107delinsTTC
XM_011545948.1:c.2112-109_2112-107delinsTTC XP_011544250.1:n.2112-109_2112-107delinsTTC
XR_950851.1:n.3793-109_3793-107delinsTTC
XM_011545946.2:c.3003-109_3003-107delinsTTC XP_011544248.1:n.3003-109_3003-107delinsTTC
XM_011545947.2:c.3003-109_3003-107delinsTTC XP_011544249.1:n.3003-109_3003-107delinsTTC
XM_011545948.2:c.2112-109_2112-107delinsTTC XP_011544250.1:n.2112-109_2112-107delinsTTC
XM_017023671.1:c.3003-109_3003-107delinsTTC XP_016879160.1:n.3003-109_3003-107delinsTTC
XM_017023672.2:c.2997-109_2997-107delinsTTC XP_016879161.1:n.2997-109_2997-107delinsTTC
XM_017023673.2:c.2997-109_2997-107delinsTTC XP_016879162.1:n.2997-109_2997-107delinsTTC
NM_024675.4:c.2997-109_2997-107delinsTTC MANE Select NP_078951.2:n.2997-109_2997-107delinsTTC