Canonical Allele Identifier: CA2731943726

Gene: PALB2

Linked Data

• dbSNP Id: rs2140960448

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641165G>T , CM000678.2:g.23641165G>T	GRCh38
NC_000016.9:g.23652486G>T , CM000678.1:g.23652486G>T	GRCh37
NC_000016.8:g.23559987G>T	NCBI36
NG_007406.1:g.5193C>A , LRG_308:g.5193C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.-860C>A	ENSP00000460666.3:n.-860C>A
ENST00000565038.2:c.-8C>A	ENSP00000459882.2:n.-8C>A
ENST00000566069.6:c.-8C>A	ENSP00000459237.2:n.-8C>A
ENST00000697377.2:c.-247C>A	ENSP00000513286.2:n.-247C>A
ENST00000697379.2:c.-153C>A	ENSP00000513287.2:n.-153C>A
ENST00000561514.2:c.-1751C>A	ENSP00000460666.2:n.-1751C>A
ENST00000697374.1:c.-1342C>A	ENSP00000513284.1:n.-1342C>A
ENST00000697376.1:c.-1063C>A	ENSP00000513285.1:n.-1063C>A
ENST00000697377.1:c.-1138C>A	ENSP00000513286.1:n.-1138C>A
ENST00000697379.1:c.-1044C>A	ENSP00000513287.1:n.-1044C>A
ENST00000697382.1:c.-1802C>A	ENSP00000513288.1:n.-1802C>A
ENST00000697383.1:c.-8C>A	ENSP00000513289.1:n.-8C>A
ENST00000697384.1:n.147C>A
ENST00000261584.9:c.-8C>A MANE Select	ENSP00000261584.4:n.-8C>A
ENST00000261584.8:c.-8C>A	ENSP00000261584.4:n.-8C>A
ENST00000567003.1:n.137C>A
ENST00000568219.5:c.-876C>A	ENSP00000454703.2:n.-876C>A
NM_024675.3:c.-8C>A , LRG_308t1:c.-8C>A	NP_078951.2:n.-8C>A
XM_011545948.1:c.-1027C>A	XP_011544250.1:n.-1027C>A
XM_011545946.2:c.-860C>A	XP_011544248.1:n.-860C>A
XM_011545947.2:c.-860C>A	XP_011544249.1:n.-860C>A
XM_011545948.2:c.-1027C>A	XP_011544250.1:n.-1027C>A
XM_017023671.1:c.-860C>A	XP_016879160.1:n.-860C>A
XM_017023672.2:c.-8C>A	XP_016879161.1:n.-8C>A
XM_017023673.2:c.-8C>A	XP_016879162.1:n.-8C>A
NM_024675.4:c.-8C>A MANE Select	NP_078951.2:n.-8C>A