Canonical Allele Identifier: CA2213410400
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621478T= , CM000678.2:g.23621478T= GRCh38
NC_000016.9:g.23632799T= , CM000678.1:g.23632799T= GRCh37
NC_000016.8:g.23540300T= NCBI36
NG_007406.1:g.24880A= , LRG_308:g.24880A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3003A= ENSP00000460666.3:p.Gly1001=
ENST00000565038.2:c.*478A= ENSP00000459882.2:n.*478A=
ENST00000566069.6:c.2997A= ENSP00000459237.2:p.Gly999=
ENST00000697377.2:c.2841A= ENSP00000513286.2:p.Gly947=
ENST00000697379.2:c.3003A= ENSP00000513287.2:p.Gly1001=
ENST00000561514.2:c.2112A= ENSP00000460666.2:p.Gly704=
ENST00000697374.1:c.2112A= ENSP00000513284.1:p.Gly704=
ENST00000697375.1:n.4344A=
ENST00000697376.1:c.2112A= ENSP00000513285.1:p.Gly704=
ENST00000697377.1:c.1950A= ENSP00000513286.1:p.Gly650=
ENST00000697378.1:n.3517A=
ENST00000697379.1:c.2112A= ENSP00000513287.1:p.Gly704=
ENST00000697380.1:n.2289A=
ENST00000697381.1:n.1692A=
ENST00000697382.1:c.2112A= ENSP00000513288.1:p.Gly704=
ENST00000697383.1:c.531A= ENSP00000513289.1:p.Gly177=
ENST00000261584.9:c.2997A= MANE Select ENSP00000261584.4:p.Gly999=
ENST00000261584.8:c.2997A= ENSP00000261584.4:p.Gly999=
ENST00000568219.5:c.2112A= ENSP00000454703.2:p.Gly704=
NM_024675.3:c.2997A= , LRG_308t1:c.2997A= NP_078951.2:p.Gly999=
XM_011545946.1:c.3003A= XP_011544248.1:p.Gly1001=
XM_011545947.1:c.3003A= XP_011544249.1:p.Gly1001=
XM_011545948.1:c.2112A= XP_011544250.1:p.Gly704=
XR_950851.1:n.3793A=
XM_011545946.2:c.3003A= XP_011544248.1:p.Gly1001=
XM_011545947.2:c.3003A= XP_011544249.1:p.Gly1001=
XM_011545948.2:c.2112A= XP_011544250.1:p.Gly704=
XM_017023671.1:c.3003A= XP_016879160.1:p.Gly1001=
XM_017023672.2:c.2997A= XP_016879161.1:p.Gly999=
XM_017023673.2:c.2997A= XP_016879162.1:p.Gly999=
NM_024675.4:c.2997A= MANE Select NP_078951.2:p.Gly999=