Canonical Allele Identifier: CA2632331024

Gene: PALB2

Linked Data

• gnomAD v4: 16-23641179-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641179A>G , CM000678.2:g.23641179A>G	GRCh38
NC_000016.9:g.23652500A>G , CM000678.1:g.23652500A>G	GRCh37
NC_000016.8:g.23560001A>G	NCBI36
NG_007406.1:g.5179T>C , LRG_308:g.5179T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-874T>C	ENSP00000460666.3:n.-874T>C
ENST00000565038.2:c.-22T>C	ENSP00000459882.2:n.-22T>C
ENST00000566069.6:c.-22T>C	ENSP00000459237.2:n.-22T>C
ENST00000697377.2:c.-261T>C	ENSP00000513286.2:n.-261T>C
ENST00000697379.2:c.-167T>C	ENSP00000513287.2:n.-167T>C
ENST00000561514.2:c.-1765T>C	ENSP00000460666.2:n.-1765T>C
ENST00000697374.1:c.-1356T>C	ENSP00000513284.1:n.-1356T>C
ENST00000697376.1:c.-1077T>C	ENSP00000513285.1:n.-1077T>C
ENST00000697377.1:c.-1152T>C	ENSP00000513286.1:n.-1152T>C
ENST00000697379.1:c.-1058T>C	ENSP00000513287.1:n.-1058T>C
ENST00000697382.1:c.-1816T>C	ENSP00000513288.1:n.-1816T>C
ENST00000697383.1:c.-22T>C	ENSP00000513289.1:n.-22T>C
ENST00000697384.1:n.133T>C
ENST00000261584.9:c.-22T>C MANE Select	ENSP00000261584.4:n.-22T>C
ENST00000261584.8:c.-22T>C	ENSP00000261584.4:n.-22T>C
ENST00000567003.1:n.123T>C
ENST00000568219.5:c.-890T>C	ENSP00000454703.2:n.-890T>C
NM_024675.3:c.-22T>C , LRG_308t1:c.-22T>C	NP_078951.2:n.-22T>C
XM_011545948.1:c.-1041T>C	XP_011544250.1:n.-1041T>C
XM_011545946.2:c.-874T>C	XP_011544248.1:n.-874T>C
XM_011545947.2:c.-874T>C	XP_011544249.1:n.-874T>C
XM_011545948.2:c.-1041T>C	XP_011544250.1:n.-1041T>C
XM_017023671.1:c.-874T>C	XP_016879160.1:n.-874T>C
XM_017023672.2:c.-22T>C	XP_016879161.1:n.-22T>C
XM_017023673.2:c.-22T>C	XP_016879162.1:n.-22T>C
NM_024675.4:c.-22T>C MANE Select	NP_078951.2:n.-22T>C