Canonical Allele Identifier: CA192457

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641149C>T , CM000678.2:g.23641149C>T	GRCh38
NC_000016.9:g.23652470C>T , CM000678.1:g.23652470C>T	GRCh37
NC_000016.8:g.23559971C>T	NCBI36
NG_007406.1:g.5209G>A , LRG_308:g.5209G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-844G>A	ENSP00000460666.3:n.-844G>A
ENST00000565038.2:c.9G>A	ENSP00000459882.2:p.Glu3=
ENST00000566069.6:c.9G>A	ENSP00000459237.2:p.Glu3=
ENST00000697377.2:c.-231G>A	ENSP00000513286.2:n.-231G>A
ENST00000697379.2:c.-137G>A	ENSP00000513287.2:n.-137G>A
ENST00000561514.2:c.-1735G>A	ENSP00000460666.2:n.-1735G>A
ENST00000697374.1:c.-1326G>A	ENSP00000513284.1:n.-1326G>A
ENST00000697376.1:c.-1047G>A	ENSP00000513285.1:n.-1047G>A
ENST00000697377.1:c.-1122G>A	ENSP00000513286.1:n.-1122G>A
ENST00000697379.1:c.-1028G>A	ENSP00000513287.1:n.-1028G>A
ENST00000697382.1:c.-1786G>A	ENSP00000513288.1:n.-1786G>A
ENST00000697383.1:c.9G>A	ENSP00000513289.1:p.Glu3=
ENST00000697384.1:n.163G>A
ENST00000261584.9:c.9G>A MANE Select	ENSP00000261584.4:p.Glu3=
ENST00000261584.8:c.9G>A	ENSP00000261584.4:p.Glu3=
ENST00000567003.1:n.153G>A
ENST00000568219.5:c.-860G>A	ENSP00000454703.2:n.-860G>A
NM_024675.3:c.9G>A , LRG_308t1:c.9G>A	NP_078951.2:p.Glu3=
XM_011545948.1:c.-1011G>A	XP_011544250.1:n.-1011G>A
XM_011545946.2:c.-844G>A	XP_011544248.1:n.-844G>A
XM_011545947.2:c.-844G>A	XP_011544249.1:n.-844G>A
XM_011545948.2:c.-1011G>A	XP_011544250.1:n.-1011G>A
XM_017023671.1:c.-844G>A	XP_016879160.1:n.-844G>A
XM_017023672.2:c.9G>A	XP_016879161.1:p.Glu3=
XM_017023673.2:c.9G>A	XP_016879162.1:p.Glu3=
NM_024675.4:c.9G>A MANE Select	NP_078951.2:p.Glu3=