Canonical Allele Identifier: CA2213432444

Gene: PALB2

Linked Data

• ClinVar Variation Id: 1036851
• ClinVar RCV Id: RCV001339913
• dbSNP Id: rs876660215

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23614001T>C , CM000678.2:g.23614001T>C	GRCh38
NC_000016.9:g.23625322T>C , CM000678.1:g.23625322T>C	GRCh37
NC_000016.8:g.23532823T>C	NCBI36
NG_007406.1:g.32357A>G , LRG_308:g.32357A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3207+3A>G	ENSP00000460666.3:n.3207+3A>G
ENST00000565038.2:c.*682+3A>G	ENSP00000459882.2:n.*682+3A>G
ENST00000566069.6:c.3201+3A>G	ENSP00000459237.2:n.3201+3A>G
ENST00000697377.2:c.3045+3A>G	ENSP00000513286.2:n.3045+3A>G
ENST00000697379.2:c.3207+3A>G	ENSP00000513287.2:n.3207+3A>G
ENST00000561514.2:c.2316+3A>G	ENSP00000460666.2:n.2316+3A>G
ENST00000697374.1:c.2316+3A>G	ENSP00000513284.1:n.2316+3A>G
ENST00000697375.1:n.4548+3A>G
ENST00000697376.1:c.2316+3A>G	ENSP00000513285.1:n.2316+3A>G
ENST00000697377.1:c.2154+3A>G	ENSP00000513286.1:n.2154+3A>G
ENST00000697378.1:n.3721+3A>G
ENST00000697379.1:c.2316+3A>G	ENSP00000513287.1:n.2316+3A>G
ENST00000697380.1:n.2406-5989A>G
ENST00000697381.1:n.1896+3A>G
ENST00000697382.1:c.2229-5989A>G	ENSP00000513288.1:n.2229-5989A>G
ENST00000697383.1:c.735+3A>G	ENSP00000513289.1:n.735+3A>G
ENST00000261584.9:c.3201+3A>G MANE Select	ENSP00000261584.4:n.3201+3A>G
ENST00000261584.8:c.3201+3A>G	ENSP00000261584.4:n.3201+3A>G
ENST00000566069.5:c.116+3A>G
ENST00000568219.5:c.2316+3A>G	ENSP00000454703.2:n.2316+3A>G
NM_024675.3:c.3201+3A>G , LRG_308t1:c.3201+3A>G	NP_078951.2:n.3201+3A>G
XM_011545946.1:c.3207+3A>G	XP_011544248.1:n.3207+3A>G
XM_011545947.1:c.3207+3A>G	XP_011544249.1:n.3207+3A>G
XM_011545948.1:c.2316+3A>G	XP_011544250.1:n.2316+3A>G
XR_950851.1:n.3910-5989A>G
XM_011545946.2:c.3207+3A>G	XP_011544248.1:n.3207+3A>G
XM_011545947.2:c.3207+3A>G	XP_011544249.1:n.3207+3A>G
XM_011545948.2:c.2316+3A>G	XP_011544250.1:n.2316+3A>G
XM_017023671.1:c.3119+7361A>G	XP_016879160.1:n.3119+7361A>G
XM_017023672.2:c.3113+7361A>G	XP_016879161.1:n.3113+7361A>G
XM_017023673.2:c.3201+3A>G	XP_016879162.1:n.3201+3A>G
NM_024675.4:c.3201+3A>G MANE Select	NP_078951.2:n.3201+3A>G