Canonical Allele Identifier: CA1139664630

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641265G>T , CM000678.2:g.23641265G>T	GRCh38
NC_000016.9:g.23652586G>T , CM000678.1:g.23652586G>T	GRCh37
NC_000016.8:g.23560087G>T	NCBI36
NG_007406.1:g.5093C>A , LRG_308:g.5093C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-960C>A	ENSP00000460666.3:n.-960C>A
ENST00000566069.6:c.-108C>A	ENSP00000459237.2:n.-108C>A
ENST00000697377.2:c.-347C>A	ENSP00000513286.2:n.-347C>A
ENST00000697379.2:c.-253C>A	ENSP00000513287.2:n.-253C>A
ENST00000561514.2:c.-1851C>A	ENSP00000460666.2:n.-1851C>A
ENST00000697376.1:c.-1163C>A	ENSP00000513285.1:n.-1163C>A
ENST00000697377.1:c.-1238C>A	ENSP00000513286.1:n.-1238C>A
ENST00000697379.1:c.-1144C>A	ENSP00000513287.1:n.-1144C>A
ENST00000697382.1:c.-1902C>A	ENSP00000513288.1:n.-1902C>A
ENST00000697383.1:c.-108C>A	ENSP00000513289.1:n.-108C>A
ENST00000697384.1:n.47C>A
ENST00000261584.9:c.-108C>A MANE Select	ENSP00000261584.4:n.-108C>A
ENST00000261584.8:c.-108C>A	ENSP00000261584.4:n.-108C>A
ENST00000567003.1:n.37C>A
ENST00000568219.5:c.-976C>A	ENSP00000454703.2:n.-976C>A
NM_024675.3:c.-108C>A , LRG_308t1:c.-108C>A	NP_078951.2:n.-108C>A
XM_011545948.1:c.-1127C>A	XP_011544250.1:n.-1127C>A
XM_011545946.2:c.-960C>A	XP_011544248.1:n.-960C>A
XM_011545947.2:c.-960C>A	XP_011544249.1:n.-960C>A
XM_011545948.2:c.-1127C>A	XP_011544250.1:n.-1127C>A
XM_017023671.1:c.-960C>A	XP_016879160.1:n.-960C>A
XM_017023672.2:c.-108C>A	XP_016879161.1:n.-108C>A
XM_017023673.2:c.-108C>A	XP_016879162.1:n.-108C>A
NM_024675.4:c.-108C>A MANE Select	NP_078951.2:n.-108C>A