Canonical Allele Identifier: CA2632331029

Gene: PALB2

Linked Data

• dbSNP Id: rs1597106322
• gnomAD v4: 16-23641180-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641180G>C , CM000678.2:g.23641180G>C	GRCh38
NC_000016.9:g.23652501G>C , CM000678.1:g.23652501G>C	GRCh37
NC_000016.8:g.23560002G>C	NCBI36
NG_007406.1:g.5178C>G , LRG_308:g.5178C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-875C>G	ENSP00000460666.3:n.-875C>G
ENST00000565038.2:c.-23C>G	ENSP00000459882.2:n.-23C>G
ENST00000566069.6:c.-23C>G	ENSP00000459237.2:n.-23C>G
ENST00000697377.2:c.-262C>G	ENSP00000513286.2:n.-262C>G
ENST00000697379.2:c.-168C>G	ENSP00000513287.2:n.-168C>G
ENST00000561514.2:c.-1766C>G	ENSP00000460666.2:n.-1766C>G
ENST00000697374.1:c.-1357C>G	ENSP00000513284.1:n.-1357C>G
ENST00000697376.1:c.-1078C>G	ENSP00000513285.1:n.-1078C>G
ENST00000697377.1:c.-1153C>G	ENSP00000513286.1:n.-1153C>G
ENST00000697379.1:c.-1059C>G	ENSP00000513287.1:n.-1059C>G
ENST00000697382.1:c.-1817C>G	ENSP00000513288.1:n.-1817C>G
ENST00000697383.1:c.-23C>G	ENSP00000513289.1:n.-23C>G
ENST00000697384.1:n.132C>G
ENST00000261584.9:c.-23C>G MANE Select	ENSP00000261584.4:n.-23C>G
ENST00000261584.8:c.-23C>G	ENSP00000261584.4:n.-23C>G
ENST00000567003.1:n.122C>G
ENST00000568219.5:c.-891C>G	ENSP00000454703.2:n.-891C>G
NM_024675.3:c.-23C>G , LRG_308t1:c.-23C>G	NP_078951.2:n.-23C>G
XM_011545948.1:c.-1042C>G	XP_011544250.1:n.-1042C>G
XM_011545946.2:c.-875C>G	XP_011544248.1:n.-875C>G
XM_011545947.2:c.-875C>G	XP_011544249.1:n.-875C>G
XM_011545948.2:c.-1042C>G	XP_011544250.1:n.-1042C>G
XM_017023671.1:c.-875C>G	XP_016879160.1:n.-875C>G
XM_017023672.2:c.-23C>G	XP_016879161.1:n.-23C>G
XM_017023673.2:c.-23C>G	XP_016879162.1:n.-23C>G
NM_024675.4:c.-23C>G MANE Select	NP_078951.2:n.-23C>G