Canonical Allele Identifier: CA2213431412
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23635968G= , CM000678.2:g.23635968G= GRCh38
NC_000016.9:g.23647289G= , CM000678.1:g.23647289G= GRCh37
NC_000016.8:g.23554790G= NCBI36
NG_007406.1:g.10390C= , LRG_308:g.10390C=

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.584C= ENSP00000460666.3:p.Thr195=
ENST00000565038.2:c.211+1882C= ENSP00000459882.2:n.211+1882C=
ENST00000566069.6:c.578C= ENSP00000459237.2:p.Thr193=
ENST00000697377.2:c.584C= ENSP00000513286.2:p.Thr195=
ENST00000697379.2:c.584C= ENSP00000513287.2:p.Thr195=
ENST00000561514.2:c.-308C= ENSP00000460666.2:n.-308C=
ENST00000697374.1:c.-308C= ENSP00000513284.1:n.-308C=
ENST00000697375.1:n.1925C=
ENST00000697376.1:c.-308C= ENSP00000513285.1:n.-308C=
ENST00000697377.1:c.-308C= ENSP00000513286.1:n.-308C=
ENST00000697378.1:n.1098C=
ENST00000697379.1:c.-308C= ENSP00000513287.1:n.-308C=
ENST00000697382.1:c.-308C= ENSP00000513288.1:n.-308C=
ENST00000697383.1:c.48+5142C= ENSP00000513289.1:n.48+5142C=
ENST00000697384.1:n.732C=
ENST00000261584.9:c.578C= MANE Select ENSP00000261584.4:p.Thr193=
ENST00000261584.8:c.578C= ENSP00000261584.4:p.Thr193=
ENST00000565038.1:c.86+1882C=
ENST00000568219.5:c.-308C= ENSP00000454703.2:n.-308C=
NM_024675.3:c.578C= , LRG_308t1:c.578C= NP_078951.2:p.Thr193=
XM_011545946.1:c.584C= XP_011544248.1:p.Thr195=
XM_011545947.1:c.584C= XP_011544249.1:p.Thr195=
XM_011545948.1:c.-308C= XP_011544250.1:n.-308C=
XR_950851.1:n.1374C=
XM_011545946.2:c.584C= XP_011544248.1:p.Thr195=
XM_011545947.2:c.584C= XP_011544249.1:p.Thr195=
XM_011545948.2:c.-308C= XP_011544250.1:n.-308C=
XM_017023671.1:c.584C= XP_016879160.1:p.Thr195=
XM_017023672.2:c.578C= XP_016879161.1:p.Thr193=
XM_017023673.2:c.578C= XP_016879162.1:p.Thr193=
NM_024675.4:c.578C= MANE Select NP_078951.2:p.Thr193=