Canonical Allele Identifier: CA2632330992

Gene: PALB2

Linked Data

• gnomAD v4: 16-23641164-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641164G>C , CM000678.2:g.23641164G>C	GRCh38
NC_000016.9:g.23652485G>C , CM000678.1:g.23652485G>C	GRCh37
NC_000016.8:g.23559986G>C	NCBI36
NG_007406.1:g.5194C>G , LRG_308:g.5194C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.-859C>G	ENSP00000460666.3:n.-859C>G
ENST00000565038.2:c.-7C>G	ENSP00000459882.2:n.-7C>G
ENST00000566069.6:c.-7C>G	ENSP00000459237.2:n.-7C>G
ENST00000697377.2:c.-246C>G	ENSP00000513286.2:n.-246C>G
ENST00000697379.2:c.-152C>G	ENSP00000513287.2:n.-152C>G
ENST00000561514.2:c.-1750C>G	ENSP00000460666.2:n.-1750C>G
ENST00000697374.1:c.-1341C>G	ENSP00000513284.1:n.-1341C>G
ENST00000697376.1:c.-1062C>G	ENSP00000513285.1:n.-1062C>G
ENST00000697377.1:c.-1137C>G	ENSP00000513286.1:n.-1137C>G
ENST00000697379.1:c.-1043C>G	ENSP00000513287.1:n.-1043C>G
ENST00000697382.1:c.-1801C>G	ENSP00000513288.1:n.-1801C>G
ENST00000697383.1:c.-7C>G	ENSP00000513289.1:n.-7C>G
ENST00000697384.1:n.148C>G
ENST00000261584.9:c.-7C>G MANE Select	ENSP00000261584.4:n.-7C>G
ENST00000261584.8:c.-7C>G	ENSP00000261584.4:n.-7C>G
ENST00000567003.1:n.138C>G
ENST00000568219.5:c.-875C>G	ENSP00000454703.2:n.-875C>G
NM_024675.3:c.-7C>G , LRG_308t1:c.-7C>G	NP_078951.2:n.-7C>G
XM_011545948.1:c.-1026C>G	XP_011544250.1:n.-1026C>G
XM_011545946.2:c.-859C>G	XP_011544248.1:n.-859C>G
XM_011545947.2:c.-859C>G	XP_011544249.1:n.-859C>G
XM_011545948.2:c.-1026C>G	XP_011544250.1:n.-1026C>G
XM_017023671.1:c.-859C>G	XP_016879160.1:n.-859C>G
XM_017023672.2:c.-7C>G	XP_016879161.1:n.-7C>G
XM_017023673.2:c.-7C>G	XP_016879162.1:n.-7C>G
NM_024675.4:c.-7C>G MANE Select	NP_078951.2:n.-7C>G