Canonical Allele Identifier: CA2806270234
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621593_23621594insCACCAAACAC , CM000678.2:g.23621593_23621594insCACCAAACAC GRCh38
NC_000016.9:g.23632914_23632915insCACCAAACAC , CM000678.1:g.23632914_23632915insCACCAAACAC GRCh37
NC_000016.8:g.23540415_23540416insCACCAAACAC NCBI36
NG_007406.1:g.24764_24765insGTGTTTGGTG , LRG_308:g.24764_24765insGTGTTTGGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3003-116_3003-115insGTGTTTGGTG ENSP00000460666.3:n.3003-116_3003-115insGTGTTTGGTG
ENST00000565038.2:c.*478-116_*478-115insGTGTTTGGTG ENSP00000459882.2:n.*478-116_*478-115insGTGTTTGGTG
ENST00000566069.6:c.2997-116_2997-115insGTGTTTGGTG ENSP00000459237.2:n.2997-116_2997-115insGTGTTTGGTG
ENST00000697377.2:c.2841-116_2841-115insGTGTTTGGTG ENSP00000513286.2:n.2841-116_2841-115insGTGTTTGGTG
ENST00000697379.2:c.3003-116_3003-115insGTGTTTGGTG ENSP00000513287.2:n.3003-116_3003-115insGTGTTTGGTG
ENST00000561514.2:c.2112-116_2112-115insGTGTTTGGTG ENSP00000460666.2:n.2112-116_2112-115insGTGTTTGGTG
ENST00000697374.1:c.2112-116_2112-115insGTGTTTGGTG ENSP00000513284.1:n.2112-116_2112-115insGTGTTTGGTG
ENST00000697375.1:n.4344-116_4344-115insGTGTTTGGTG
ENST00000697376.1:c.2112-116_2112-115insGTGTTTGGTG ENSP00000513285.1:n.2112-116_2112-115insGTGTTTGGTG
ENST00000697377.1:c.1950-116_1950-115insGTGTTTGGTG ENSP00000513286.1:n.1950-116_1950-115insGTGTTTGGTG
ENST00000697378.1:n.3517-116_3517-115insGTGTTTGGTG
ENST00000697379.1:c.2112-116_2112-115insGTGTTTGGTG ENSP00000513287.1:n.2112-116_2112-115insGTGTTTGGTG
ENST00000697380.1:n.2289-116_2289-115insGTGTTTGGTG
ENST00000697381.1:n.1692-116_1692-115insGTGTTTGGTG
ENST00000697382.1:c.2112-116_2112-115insGTGTTTGGTG ENSP00000513288.1:n.2112-116_2112-115insGTGTTTGGTG
ENST00000697383.1:c.531-116_531-115insGTGTTTGGTG ENSP00000513289.1:n.531-116_531-115insGTGTTTGGTG
ENST00000261584.9:c.2997-116_2997-115insGTGTTTGGTG MANE Select ENSP00000261584.4:n.2997-116_2997-115insGTGTTTGGTG
ENST00000261584.8:c.2997-116_2997-115insGTGTTTGGTG ENSP00000261584.4:n.2997-116_2997-115insGTGTTTGGTG
ENST00000568219.5:c.2112-116_2112-115insGTGTTTGGTG ENSP00000454703.2:n.2112-116_2112-115insGTGTTTGGTG
NM_024675.3:c.2997-116_2997-115insGTGTTTGGTG , LRG_308t1:c.2997-116_2997-115insGTGTTTGGTG NP_078951.2:n.2997-116_2997-115insGTGTTTGGTG
XM_011545946.1:c.3003-116_3003-115insGTGTTTGGTG XP_011544248.1:n.3003-116_3003-115insGTGTTTGGTG
XM_011545947.1:c.3003-116_3003-115insGTGTTTGGTG XP_011544249.1:n.3003-116_3003-115insGTGTTTGGTG
XM_011545948.1:c.2112-116_2112-115insGTGTTTGGTG XP_011544250.1:n.2112-116_2112-115insGTGTTTGGTG
XR_950851.1:n.3793-116_3793-115insGTGTTTGGTG
XM_011545946.2:c.3003-116_3003-115insGTGTTTGGTG XP_011544248.1:n.3003-116_3003-115insGTGTTTGGTG
XM_011545947.2:c.3003-116_3003-115insGTGTTTGGTG XP_011544249.1:n.3003-116_3003-115insGTGTTTGGTG
XM_011545948.2:c.2112-116_2112-115insGTGTTTGGTG XP_011544250.1:n.2112-116_2112-115insGTGTTTGGTG
XM_017023671.1:c.3003-116_3003-115insGTGTTTGGTG XP_016879160.1:n.3003-116_3003-115insGTGTTTGGTG
XM_017023672.2:c.2997-116_2997-115insGTGTTTGGTG XP_016879161.1:n.2997-116_2997-115insGTGTTTGGTG
XM_017023673.2:c.2997-116_2997-115insGTGTTTGGTG XP_016879162.1:n.2997-116_2997-115insGTGTTTGGTG
NM_024675.4:c.2997-116_2997-115insGTGTTTGGTG MANE Select NP_078951.2:n.2997-116_2997-115insGTGTTTGGTG