Canonical Allele Identifier: CA2213424196
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23603371T= , CM000678.2:g.23603371T= GRCh38
NC_000016.9:g.23614692T= , CM000678.1:g.23614692T= GRCh37
NC_000016.8:g.23522193T= NCBI36
NG_007406.1:g.42987A= , LRG_308:g.42987A=

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.*88A= ENSP00000460666.3:n.*88A=
ENST00000565038.2:c.*1134A= ENSP00000459882.2:n.*1134A=
ENST00000566069.6:c.*284A= ENSP00000459237.2:n.*284A=
ENST00000697377.2:c.*88A= ENSP00000513286.2:n.*88A=
ENST00000697379.2:c.*88A= ENSP00000513287.2:n.*88A=
ENST00000561514.2:c.*88A= ENSP00000460666.2:n.*88A=
ENST00000697374.1:c.*88A= ENSP00000513284.1:n.*88A=
ENST00000697375.1:n.4996A=
ENST00000697376.1:c.*284A= ENSP00000513285.1:n.*284A=
ENST00000697377.1:c.*88A= ENSP00000513286.1:n.*88A=
ENST00000697378.1:n.4169A=
ENST00000697379.1:c.*88A= ENSP00000513287.1:n.*88A=
ENST00000697380.1:n.2853A=
ENST00000697381.1:n.2344A=
ENST00000697382.1:c.*426A= ENSP00000513288.1:n.*426A=
ENST00000697383.1:c.*88A= ENSP00000513289.1:n.*88A=
ENST00000261584.9:c.*88A= MANE Select ENSP00000261584.4:n.*88A=
ENST00000261584.8:c.*88A= ENSP00000261584.4:n.*88A=
ENST00000566069.5:c.415A=
ENST00000568219.5:c.*88A= ENSP00000454703.2:n.*88A=
NM_024675.3:c.*88A= , LRG_308t1:c.*88A= NP_078951.2:n.*88A=
XM_011545946.1:c.*88A= XP_011544248.1:n.*88A=
XM_011545947.1:c.*284A= XP_011544249.1:n.*284A=
XM_011545948.1:c.*88A= XP_011544250.1:n.*88A=
XR_950851.1:n.4357A=
XM_011545946.2:c.*88A= XP_011544248.1:n.*88A=
XM_011545947.2:c.*284A= XP_011544249.1:n.*284A=
XM_011545948.2:c.*88A= XP_011544250.1:n.*88A=
XM_017023671.1:c.*88A= XP_016879160.1:n.*88A=
XM_017023672.2:c.*88A= XP_016879161.1:n.*88A=
XM_017023673.2:c.*284A= XP_016879162.1:n.*284A=
NM_024675.4:c.*88A= MANE Select NP_078951.2:n.*88A=