Canonical Allele Identifier: CA2632331005

Gene: PALB2

Linked Data

• gnomAD v4: 16-23641169-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641169C>A , CM000678.2:g.23641169C>A	GRCh38
NC_000016.9:g.23652490C>A , CM000678.1:g.23652490C>A	GRCh37
NC_000016.8:g.23559991C>A	NCBI36
NG_007406.1:g.5189G>T , LRG_308:g.5189G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-864G>T	ENSP00000460666.3:n.-864G>T
ENST00000565038.2:c.-12G>T	ENSP00000459882.2:n.-12G>T
ENST00000566069.6:c.-12G>T	ENSP00000459237.2:n.-12G>T
ENST00000697377.2:c.-251G>T	ENSP00000513286.2:n.-251G>T
ENST00000697379.2:c.-157G>T	ENSP00000513287.2:n.-157G>T
ENST00000561514.2:c.-1755G>T	ENSP00000460666.2:n.-1755G>T
ENST00000697374.1:c.-1346G>T	ENSP00000513284.1:n.-1346G>T
ENST00000697376.1:c.-1067G>T	ENSP00000513285.1:n.-1067G>T
ENST00000697377.1:c.-1142G>T	ENSP00000513286.1:n.-1142G>T
ENST00000697379.1:c.-1048G>T	ENSP00000513287.1:n.-1048G>T
ENST00000697382.1:c.-1806G>T	ENSP00000513288.1:n.-1806G>T
ENST00000697383.1:c.-12G>T	ENSP00000513289.1:n.-12G>T
ENST00000697384.1:n.143G>T
ENST00000261584.9:c.-12G>T MANE Select	ENSP00000261584.4:n.-12G>T
ENST00000261584.8:c.-12G>T	ENSP00000261584.4:n.-12G>T
ENST00000567003.1:n.133G>T
ENST00000568219.5:c.-880G>T	ENSP00000454703.2:n.-880G>T
NM_024675.3:c.-12G>T , LRG_308t1:c.-12G>T	NP_078951.2:n.-12G>T
XM_011545948.1:c.-1031G>T	XP_011544250.1:n.-1031G>T
XM_011545946.2:c.-864G>T	XP_011544248.1:n.-864G>T
XM_011545947.2:c.-864G>T	XP_011544249.1:n.-864G>T
XM_011545948.2:c.-1031G>T	XP_011544250.1:n.-1031G>T
XM_017023671.1:c.-864G>T	XP_016879160.1:n.-864G>T
XM_017023672.2:c.-12G>T	XP_016879161.1:n.-12G>T
XM_017023673.2:c.-12G>T	XP_016879162.1:n.-12G>T
NM_024675.4:c.-12G>T MANE Select	NP_078951.2:n.-12G>T