Canonical Allele Identifier: CA2731900633
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs1233575092

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23613982G>C , CM000678.2:g.23613982G>C GRCh38
NC_000016.9:g.23625303G>C , CM000678.1:g.23625303G>C GRCh37
NC_000016.8:g.23532804G>C NCBI36
NG_007406.1:g.32376C>G , LRG_308:g.32376C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.3207+22C>G ENSP00000460666.3:n.3207+22C>G
ENST00000565038.2:c.*682+22C>G ENSP00000459882.2:n.*682+22C>G
ENST00000566069.6:c.3201+22C>G ENSP00000459237.2:n.3201+22C>G
ENST00000697377.2:c.3045+22C>G ENSP00000513286.2:n.3045+22C>G
ENST00000697379.2:c.3207+22C>G ENSP00000513287.2:n.3207+22C>G
ENST00000561514.2:c.2316+22C>G ENSP00000460666.2:n.2316+22C>G
ENST00000697374.1:c.2316+22C>G ENSP00000513284.1:n.2316+22C>G
ENST00000697375.1:n.4548+22C>G
ENST00000697376.1:c.2316+22C>G ENSP00000513285.1:n.2316+22C>G
ENST00000697377.1:c.2154+22C>G ENSP00000513286.1:n.2154+22C>G
ENST00000697378.1:n.3721+22C>G
ENST00000697379.1:c.2316+22C>G ENSP00000513287.1:n.2316+22C>G
ENST00000697380.1:n.2406-5970C>G
ENST00000697381.1:n.1896+22C>G
ENST00000697382.1:c.2229-5970C>G ENSP00000513288.1:n.2229-5970C>G
ENST00000697383.1:c.735+22C>G ENSP00000513289.1:n.735+22C>G
ENST00000261584.9:c.3201+22C>G MANE Select ENSP00000261584.4:n.3201+22C>G
ENST00000261584.8:c.3201+22C>G ENSP00000261584.4:n.3201+22C>G
ENST00000566069.5:c.116+22C>G
ENST00000568219.5:c.2316+22C>G ENSP00000454703.2:n.2316+22C>G
NM_024675.3:c.3201+22C>G , LRG_308t1:c.3201+22C>G NP_078951.2:n.3201+22C>G
XM_011545946.1:c.3207+22C>G XP_011544248.1:n.3207+22C>G
XM_011545947.1:c.3207+22C>G XP_011544249.1:n.3207+22C>G
XM_011545948.1:c.2316+22C>G XP_011544250.1:n.2316+22C>G
XR_950851.1:n.3910-5970C>G
XM_011545946.2:c.3207+22C>G XP_011544248.1:n.3207+22C>G
XM_011545947.2:c.3207+22C>G XP_011544249.1:n.3207+22C>G
XM_011545948.2:c.2316+22C>G XP_011544250.1:n.2316+22C>G
XM_017023671.1:c.3119+7380C>G XP_016879160.1:n.3119+7380C>G
XM_017023672.2:c.3113+7380C>G XP_016879161.1:n.3113+7380C>G
XM_017023673.2:c.3201+22C>G XP_016879162.1:n.3201+22C>G
NM_024675.4:c.3201+22C>G MANE Select NP_078951.2:n.3201+22C>G