Canonical Allele Identifier: CA2632329000

Gene: PALB2

Linked Data

• gnomAD v4: 16-23641270-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641270G>T , CM000678.2:g.23641270G>T	GRCh38
NC_000016.9:g.23652591G>T , CM000678.1:g.23652591G>T	GRCh37
NC_000016.8:g.23560092G>T	NCBI36
NG_007406.1:g.5088C>A , LRG_308:g.5088C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-965C>A	ENSP00000460666.3:n.-965C>A
ENST00000566069.6:c.-113C>A	ENSP00000459237.2:n.-113C>A
ENST00000697377.2:c.-352C>A	ENSP00000513286.2:n.-352C>A
ENST00000697379.2:c.-258C>A	ENSP00000513287.2:n.-258C>A
ENST00000561514.2:c.-1856C>A	ENSP00000460666.2:n.-1856C>A
ENST00000697376.1:c.-1168C>A	ENSP00000513285.1:n.-1168C>A
ENST00000697377.1:c.-1243C>A	ENSP00000513286.1:n.-1243C>A
ENST00000697379.1:c.-1149C>A	ENSP00000513287.1:n.-1149C>A
ENST00000697382.1:c.-1907C>A	ENSP00000513288.1:n.-1907C>A
ENST00000697383.1:c.-113C>A	ENSP00000513289.1:n.-113C>A
ENST00000697384.1:n.42C>A
ENST00000261584.9:c.-113C>A MANE Select	ENSP00000261584.4:n.-113C>A
ENST00000261584.8:c.-113C>A	ENSP00000261584.4:n.-113C>A
ENST00000567003.1:n.32C>A
ENST00000568219.5:c.-981C>A	ENSP00000454703.2:n.-981C>A
NM_024675.3:c.-113C>A , LRG_308t1:c.-113C>A	NP_078951.2:n.-113C>A
XM_011545948.1:c.-1132C>A	XP_011544250.1:n.-1132C>A
XM_011545946.2:c.-965C>A	XP_011544248.1:n.-965C>A
XM_011545948.2:c.-1132C>A	XP_011544250.1:n.-1132C>A
XM_017023672.2:c.-113C>A	XP_016879161.1:n.-113C>A
XM_017023673.2:c.-113C>A	XP_016879162.1:n.-113C>A
NM_024675.4:c.-113C>A MANE Select	NP_078951.2:n.-113C>A