Canonical Allele Identifier: CA494168496

Gene: PALB2

Linked Data

• dbSNP Id: rs567706422
• MyVariant Identifiers: chr16:g.23652467A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641146A>T , CM000678.2:g.23641146A>T	GRCh38
NC_000016.9:g.23652467A>T , CM000678.1:g.23652467A>T	GRCh37
NC_000016.8:g.23559968A>T	NCBI36
NG_007406.1:g.5212T>A , LRG_308:g.5212T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-841T>A	ENSP00000460666.3:n.-841T>A
ENST00000565038.2:c.12T>A	ENSP00000459882.2:p.Pro4=
ENST00000566069.6:c.12T>A	ENSP00000459237.2:p.Pro4=
ENST00000697377.2:c.-228T>A	ENSP00000513286.2:n.-228T>A
ENST00000697379.2:c.-134T>A	ENSP00000513287.2:n.-134T>A
ENST00000561514.2:c.-1732T>A	ENSP00000460666.2:n.-1732T>A
ENST00000697374.1:c.-1323T>A	ENSP00000513284.1:n.-1323T>A
ENST00000697376.1:c.-1044T>A	ENSP00000513285.1:n.-1044T>A
ENST00000697377.1:c.-1119T>A	ENSP00000513286.1:n.-1119T>A
ENST00000697379.1:c.-1025T>A	ENSP00000513287.1:n.-1025T>A
ENST00000697382.1:c.-1783T>A	ENSP00000513288.1:n.-1783T>A
ENST00000697383.1:c.12T>A	ENSP00000513289.1:p.Pro4=
ENST00000697384.1:n.166T>A
ENST00000261584.9:c.12T>A MANE Select	ENSP00000261584.4:p.Pro4=
ENST00000261584.8:c.12T>A	ENSP00000261584.4:p.Pro4=
ENST00000567003.1:n.156T>A
ENST00000568219.5:c.-857T>A	ENSP00000454703.2:n.-857T>A
NM_024675.3:c.12T>A , LRG_308t1:c.12T>A	NP_078951.2:p.Pro4=
XM_011545948.1:c.-1008T>A	XP_011544250.1:n.-1008T>A
XM_011545946.2:c.-841T>A	XP_011544248.1:n.-841T>A
XM_011545947.2:c.-841T>A	XP_011544249.1:n.-841T>A
XM_011545948.2:c.-1008T>A	XP_011544250.1:n.-1008T>A
XM_017023671.1:c.-841T>A	XP_016879160.1:n.-841T>A
XM_017023672.2:c.12T>A	XP_016879161.1:p.Pro4=
XM_017023673.2:c.12T>A	XP_016879162.1:p.Pro4=
NM_024675.4:c.12T>A MANE Select	NP_078951.2:p.Pro4=