Canonical Allele Identifier: CA2632331011

Gene: PALB2

Linked Data

• dbSNP Id: rs2140960520
• gnomAD v4: 16-23641173-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641173A>C , CM000678.2:g.23641173A>C	GRCh38
NC_000016.9:g.23652494A>C , CM000678.1:g.23652494A>C	GRCh37
NC_000016.8:g.23559995A>C	NCBI36
NG_007406.1:g.5185T>G , LRG_308:g.5185T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-868T>G	ENSP00000460666.3:n.-868T>G
ENST00000565038.2:c.-16T>G	ENSP00000459882.2:n.-16T>G
ENST00000566069.6:c.-16T>G	ENSP00000459237.2:n.-16T>G
ENST00000697377.2:c.-255T>G	ENSP00000513286.2:n.-255T>G
ENST00000697379.2:c.-161T>G	ENSP00000513287.2:n.-161T>G
ENST00000561514.2:c.-1759T>G	ENSP00000460666.2:n.-1759T>G
ENST00000697374.1:c.-1350T>G	ENSP00000513284.1:n.-1350T>G
ENST00000697376.1:c.-1071T>G	ENSP00000513285.1:n.-1071T>G
ENST00000697377.1:c.-1146T>G	ENSP00000513286.1:n.-1146T>G
ENST00000697379.1:c.-1052T>G	ENSP00000513287.1:n.-1052T>G
ENST00000697382.1:c.-1810T>G	ENSP00000513288.1:n.-1810T>G
ENST00000697383.1:c.-16T>G	ENSP00000513289.1:n.-16T>G
ENST00000697384.1:n.139T>G
ENST00000261584.9:c.-16T>G MANE Select	ENSP00000261584.4:n.-16T>G
ENST00000261584.8:c.-16T>G	ENSP00000261584.4:n.-16T>G
ENST00000567003.1:n.129T>G
ENST00000568219.5:c.-884T>G	ENSP00000454703.2:n.-884T>G
NM_024675.3:c.-16T>G , LRG_308t1:c.-16T>G	NP_078951.2:n.-16T>G
XM_011545948.1:c.-1035T>G	XP_011544250.1:n.-1035T>G
XM_011545946.2:c.-868T>G	XP_011544248.1:n.-868T>G
XM_011545947.2:c.-868T>G	XP_011544249.1:n.-868T>G
XM_011545948.2:c.-1035T>G	XP_011544250.1:n.-1035T>G
XM_017023671.1:c.-868T>G	XP_016879160.1:n.-868T>G
XM_017023672.2:c.-16T>G	XP_016879161.1:n.-16T>G
XM_017023673.2:c.-16T>G	XP_016879162.1:n.-16T>G
NM_024675.4:c.-16T>G MANE Select	NP_078951.2:n.-16T>G