Canonical Allele Identifier: CA395137643
Gene: PALB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23603470G>C , CM000678.2:g.23603470G>C GRCh38
NC_000016.9:g.23614791G>C , CM000678.1:g.23614791G>C GRCh37
NC_000016.8:g.23522292G>C NCBI36
NG_007406.1:g.42888C>G , LRG_308:g.42888C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3556C>G ENSP00000460666.3:p.His1186Asp
ENST00000565038.2:c.*1035C>G ENSP00000459882.2:n.*1035C>G
ENST00000566069.6:c.*185C>G ENSP00000459237.2:n.*185C>G
ENST00000697377.2:c.3394C>G ENSP00000513286.2:p.His1132Asp
ENST00000697379.2:c.3556C>G ENSP00000513287.2:p.His1186Asp
ENST00000561514.2:c.2665C>G ENSP00000460666.2:p.His889Asp
ENST00000697374.1:c.2665C>G ENSP00000513284.1:p.His889Asp
ENST00000697375.1:n.4897C>G
ENST00000697376.1:c.*185C>G ENSP00000513285.1:n.*185C>G
ENST00000697377.1:c.2503C>G ENSP00000513286.1:p.His835Asp
ENST00000697378.1:n.4070C>G
ENST00000697379.1:c.2665C>G ENSP00000513287.1:p.His889Asp
ENST00000697380.1:n.2754C>G
ENST00000697381.1:n.2245C>G
ENST00000697382.1:c.*327C>G ENSP00000513288.1:n.*327C>G
ENST00000697383.1:c.1084C>G ENSP00000513289.1:p.His362Asp
ENST00000261584.9:c.3550C>G MANE Select ENSP00000261584.4:p.His1184Asp
ENST00000261584.8:c.3550C>G ENSP00000261584.4:p.His1184Asp
ENST00000566069.5:c.316C>G
ENST00000568219.5:c.2665C>G ENSP00000454703.2:p.His889Asp
NM_024675.3:c.3550C>G , LRG_308t1:c.3550C>G NP_078951.2:p.His1184Asp
XM_011545946.1:c.3556C>G XP_011544248.1:p.His1186Asp
XM_011545947.1:c.*185C>G XP_011544249.1:n.*185C>G
XM_011545948.1:c.2665C>G XP_011544250.1:p.His889Asp
XR_950851.1:n.4258C>G
XM_011545946.2:c.3556C>G XP_011544248.1:p.His1186Asp
XM_011545947.2:c.*185C>G XP_011544249.1:n.*185C>G
XM_011545948.2:c.2665C>G XP_011544250.1:p.His889Asp
XM_017023671.1:c.3319C>G XP_016879160.1:p.His1107Asp
XM_017023672.2:c.3313C>G XP_016879161.1:p.His1105Asp
XM_017023673.2:c.*185C>G XP_016879162.1:n.*185C>G
NM_024675.4:c.3550C>G MANE Select NP_078951.2:p.His1184Asp