Canonical Allele Identifier: CA395144089
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs2142335470

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23623020C>T , CM000678.2:g.23623020C>T GRCh38
NC_000016.9:g.23634341C>T , CM000678.1:g.23634341C>T GRCh37
NC_000016.8:g.23541842C>T NCBI36
NG_007406.1:g.23338G>A , LRG_308:g.23338G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.2951G>A ENSP00000460666.3:p.Gly984Glu
ENST00000565038.2:c.*426G>A ENSP00000459882.2:n.*426G>A
ENST00000566069.6:c.2945G>A ENSP00000459237.2:p.Gly982Glu
ENST00000697377.2:c.2789G>A ENSP00000513286.2:p.Gly930Glu
ENST00000697379.2:c.2951G>A ENSP00000513287.2:p.Gly984Glu
ENST00000561514.2:c.2060G>A ENSP00000460666.2:p.Gly687Glu
ENST00000697374.1:c.2060G>A ENSP00000513284.1:p.Gly687Glu
ENST00000697375.1:n.4292G>A
ENST00000697376.1:c.2060G>A ENSP00000513285.1:p.Gly687Glu
ENST00000697377.1:c.1898G>A ENSP00000513286.1:p.Gly633Glu
ENST00000697378.1:n.3465G>A
ENST00000697379.1:c.2060G>A ENSP00000513287.1:p.Gly687Glu
ENST00000697380.1:n.2237G>A
ENST00000697381.1:n.1640G>A
ENST00000697382.1:c.2060G>A ENSP00000513288.1:p.Gly687Glu
ENST00000697383.1:c.479G>A ENSP00000513289.1:p.Gly160Glu
ENST00000261584.9:c.2945G>A MANE Select ENSP00000261584.4:p.Gly982Glu
ENST00000261584.8:c.2945G>A ENSP00000261584.4:p.Gly982Glu
ENST00000568219.5:c.2060G>A ENSP00000454703.2:p.Gly687Glu
NM_024675.3:c.2945G>A , LRG_308t1:c.2945G>A NP_078951.2:p.Gly982Glu
XM_011545946.1:c.2951G>A XP_011544248.1:p.Gly984Glu
XM_011545947.1:c.2951G>A XP_011544249.1:p.Gly984Glu
XM_011545948.1:c.2060G>A XP_011544250.1:p.Gly687Glu
XR_950851.1:n.3741G>A
XM_011545946.2:c.2951G>A XP_011544248.1:p.Gly984Glu
XM_011545947.2:c.2951G>A XP_011544249.1:p.Gly984Glu
XM_011545948.2:c.2060G>A XP_011544250.1:p.Gly687Glu
XM_017023671.1:c.2951G>A XP_016879160.1:p.Gly984Glu
XM_017023672.2:c.2945G>A XP_016879161.1:p.Gly982Glu
XM_017023673.2:c.2945G>A XP_016879162.1:p.Gly982Glu
NM_024675.4:c.2945G>A MANE Select NP_078951.2:p.Gly982Glu