Canonical Allele Identifier: CA2632330994

Gene: PALB2

Linked Data

• gnomAD v4: 16-23641166-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641166C>A , CM000678.2:g.23641166C>A	GRCh38
NC_000016.9:g.23652487C>A , CM000678.1:g.23652487C>A	GRCh37
NC_000016.8:g.23559988C>A	NCBI36
NG_007406.1:g.5192G>T , LRG_308:g.5192G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.-861G>T	ENSP00000460666.3:n.-861G>T
ENST00000565038.2:c.-9G>T	ENSP00000459882.2:n.-9G>T
ENST00000566069.6:c.-9G>T	ENSP00000459237.2:n.-9G>T
ENST00000697377.2:c.-248G>T	ENSP00000513286.2:n.-248G>T
ENST00000697379.2:c.-154G>T	ENSP00000513287.2:n.-154G>T
ENST00000561514.2:c.-1752G>T	ENSP00000460666.2:n.-1752G>T
ENST00000697374.1:c.-1343G>T	ENSP00000513284.1:n.-1343G>T
ENST00000697376.1:c.-1064G>T	ENSP00000513285.1:n.-1064G>T
ENST00000697377.1:c.-1139G>T	ENSP00000513286.1:n.-1139G>T
ENST00000697379.1:c.-1045G>T	ENSP00000513287.1:n.-1045G>T
ENST00000697382.1:c.-1803G>T	ENSP00000513288.1:n.-1803G>T
ENST00000697383.1:c.-9G>T	ENSP00000513289.1:n.-9G>T
ENST00000697384.1:n.146G>T
ENST00000261584.9:c.-9G>T MANE Select	ENSP00000261584.4:n.-9G>T
ENST00000261584.8:c.-9G>T	ENSP00000261584.4:n.-9G>T
ENST00000567003.1:n.136G>T
ENST00000568219.5:c.-877G>T	ENSP00000454703.2:n.-877G>T
NM_024675.3:c.-9G>T , LRG_308t1:c.-9G>T	NP_078951.2:n.-9G>T
XM_011545948.1:c.-1028G>T	XP_011544250.1:n.-1028G>T
XM_011545946.2:c.-861G>T	XP_011544248.1:n.-861G>T
XM_011545947.2:c.-861G>T	XP_011544249.1:n.-861G>T
XM_011545948.2:c.-1028G>T	XP_011544250.1:n.-1028G>T
XM_017023671.1:c.-861G>T	XP_016879160.1:n.-861G>T
XM_017023672.2:c.-9G>T	XP_016879161.1:n.-9G>T
XM_017023673.2:c.-9G>T	XP_016879162.1:n.-9G>T
NM_024675.4:c.-9G>T MANE Select	NP_078951.2:n.-9G>T