Canonical Allele Identifier: CA2213424205
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23603401C= , CM000678.2:g.23603401C= GRCh38
NC_000016.9:g.23614722C= , CM000678.1:g.23614722C= GRCh37
NC_000016.8:g.23522223C= NCBI36
NG_007406.1:g.42957G= , LRG_308:g.42957G=

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.*58G= ENSP00000460666.3:n.*58G=
ENST00000565038.2:c.*1104G= ENSP00000459882.2:n.*1104G=
ENST00000566069.6:c.*254G= ENSP00000459237.2:n.*254G=
ENST00000697377.2:c.*58G= ENSP00000513286.2:n.*58G=
ENST00000697379.2:c.*58G= ENSP00000513287.2:n.*58G=
ENST00000561514.2:c.*58G= ENSP00000460666.2:n.*58G=
ENST00000697374.1:c.*58G= ENSP00000513284.1:n.*58G=
ENST00000697375.1:n.4966G=
ENST00000697376.1:c.*254G= ENSP00000513285.1:n.*254G=
ENST00000697377.1:c.*58G= ENSP00000513286.1:n.*58G=
ENST00000697378.1:n.4139G=
ENST00000697379.1:c.*58G= ENSP00000513287.1:n.*58G=
ENST00000697380.1:n.2823G=
ENST00000697381.1:n.2314G=
ENST00000697382.1:c.*396G= ENSP00000513288.1:n.*396G=
ENST00000697383.1:c.*58G= ENSP00000513289.1:n.*58G=
ENST00000261584.9:c.*58G= MANE Select ENSP00000261584.4:n.*58G=
ENST00000261584.8:c.*58G= ENSP00000261584.4:n.*58G=
ENST00000566069.5:c.385G=
ENST00000568219.5:c.*58G= ENSP00000454703.2:n.*58G=
NM_024675.3:c.*58G= , LRG_308t1:c.*58G= NP_078951.2:n.*58G=
XM_011545946.1:c.*58G= XP_011544248.1:n.*58G=
XM_011545947.1:c.*254G= XP_011544249.1:n.*254G=
XM_011545948.1:c.*58G= XP_011544250.1:n.*58G=
XR_950851.1:n.4327G=
XM_011545946.2:c.*58G= XP_011544248.1:n.*58G=
XM_011545947.2:c.*254G= XP_011544249.1:n.*254G=
XM_011545948.2:c.*58G= XP_011544250.1:n.*58G=
XM_017023671.1:c.*58G= XP_016879160.1:n.*58G=
XM_017023672.2:c.*58G= XP_016879161.1:n.*58G=
XM_017023673.2:c.*254G= XP_016879162.1:n.*254G=
NM_024675.4:c.*58G= MANE Select NP_078951.2:n.*58G=