Canonical Allele Identifier: CA2213424234
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23603447_23603468delinsCTTTACCCTAACTTATGAATAG , CM000678.2:g.23603447_23603468delinsCTTTACCCTAACTTATGAATAG GRCh38
NC_000016.9:g.23614768_23614789delinsCTTTACCCTAACTTATGAATAG , CM000678.1:g.23614768_23614789delinsCTTTACCCTAACTTATGAATAG GRCh37
NC_000016.8:g.23522269_23522290delinsCTTTACCCTAACTTATGAATAG NCBI36
NG_007406.1:g.42890_42911delinsCTATTCATAAGTTAGGGTAAAG , LRG_308:g.42890_42911delinsCTATTCATAAGTTAGGGTAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3558_*12delinsCTATTCATAAGTTAGGGTAAAG ENSP00000460666.3:n.[c.3558_*12delinsCTATTCATAAGTTAGGGTAAAG;H...
ENST00000565038.2:c.*1037_*1058delinsCTATTCATAAGTTAGGGTAAAG ENSP00000459882.2:n.*1037_*1058delinsCTATTCATAAGTTAGGGTAAAG
ENST00000566069.6:c.*187_*208delinsCTATTCATAAGTTAGGGTAAAG ENSP00000459237.2:n.*187_*208delinsCTATTCATAAGTTAGGGTAAAG
ENST00000697377.2:c.3396_*12delinsCTATTCATAAGTTAGGGTAAAG ENSP00000513286.2:n.[c.3396_*12delinsCTATTCATAAGTTAGGGTAAAG;H...
ENST00000697379.2:c.3558_*12delinsCTATTCATAAGTTAGGGTAAAG ENSP00000513287.2:n.[c.3558_*12delinsCTATTCATAAGTTAGGGTAAAG;H...
ENST00000561514.2:c.2667_*12delinsCTATTCATAAGTTAGGGTAAAG ENSP00000460666.2:n.[c.2667_*12delinsCTATTCATAAGTTAGGGTAAAG;H...
ENST00000697374.1:c.2667_*12delinsCTATTCATAAGTTAGGGTAAAG ENSP00000513284.1:n.[c.2667_*12delinsCTATTCATAAGTTAGGGTAAAG;H...
ENST00000697375.1:n.4899_4920delinsCTATTCATAAGTTAGGGTAAAG
ENST00000697376.1:c.*187_*208delinsCTATTCATAAGTTAGGGTAAAG ENSP00000513285.1:n.*187_*208delinsCTATTCATAAGTTAGGGTAAAG
ENST00000697377.1:c.2505_*12delinsCTATTCATAAGTTAGGGTAAAG ENSP00000513286.1:n.[c.2505_*12delinsCTATTCATAAGTTAGGGTAAAG;H...
ENST00000697378.1:n.4072_4093delinsCTATTCATAAGTTAGGGTAAAG
ENST00000697379.1:c.2667_*12delinsCTATTCATAAGTTAGGGTAAAG ENSP00000513287.1:n.[c.2667_*12delinsCTATTCATAAGTTAGGGTAAAG;H...
ENST00000697380.1:n.2756_2777delinsCTATTCATAAGTTAGGGTAAAG
ENST00000697381.1:n.2247_2268delinsCTATTCATAAGTTAGGGTAAAG
ENST00000697382.1:c.*329_*350delinsCTATTCATAAGTTAGGGTAAAG ENSP00000513288.1:n.*329_*350delinsCTATTCATAAGTTAGGGTAAAG
ENST00000697383.1:c.1086_*12delinsCTATTCATAAGTTAGGGTAAAG ENSP00000513289.1:n.[c.1086_*12delinsCTATTCATAAGTTAGGGTAAAG;H...
ENST00000261584.9:c.3552_*12delinsCTATTCATAAGTTAGGGTAAAG MANE Select ENSP00000261584.4:n.[c.3552_*12delinsCTATTCATAAGTTAGGGTAAAG;H...
ENST00000261584.8:c.3552_*12delinsCTATTCATAAGTTAGGGTAAAG ENSP00000261584.4:n.[c.3552_*12delinsCTATTCATAAGTTAGGGTAAAG;H...
ENST00000566069.5:c.318_339delinsCTATTCATAAGTTAGGGTAAAG
ENST00000568219.5:c.2667_*12delinsCTATTCATAAGTTAGGGTAAAG ENSP00000454703.2:n.[c.2667_*12delinsCTATTCATAAGTTAGGGTAAAG;H...
NM_024675.3:c.3552_*12delinsCTATTCATAAGTTAGGGTAAAG , LRG_308t1:c.3552_*12delinsCTATTCATAAGTTAGGGTAAAG NP_078951.2:n.[c.3552_*12delinsCTATTCATAAGTTAGGGTAAAG;His1184...
XM_011545946.1:c.3558_*12delinsCTATTCATAAGTTAGGGTAAAG XP_011544248.1:n.[c.3558_*12delinsCTATTCATAAGTTAGGGTAAAG;His1...
XM_011545947.1:c.*187_*208delinsCTATTCATAAGTTAGGGTAAAG XP_011544249.1:n.*187_*208delinsCTATTCATAAGTTAGGGTAAAG
XM_011545948.1:c.2667_*12delinsCTATTCATAAGTTAGGGTAAAG XP_011544250.1:n.[c.2667_*12delinsCTATTCATAAGTTAGGGTAAAG;His8...
XR_950851.1:n.4260_4281delinsCTATTCATAAGTTAGGGTAAAG
XM_011545946.2:c.3558_*12delinsCTATTCATAAGTTAGGGTAAAG XP_011544248.1:n.[c.3558_*12delinsCTATTCATAAGTTAGGGTAAAG;His1...
XM_011545947.2:c.*187_*208delinsCTATTCATAAGTTAGGGTAAAG XP_011544249.1:n.*187_*208delinsCTATTCATAAGTTAGGGTAAAG
XM_011545948.2:c.2667_*12delinsCTATTCATAAGTTAGGGTAAAG XP_011544250.1:n.[c.2667_*12delinsCTATTCATAAGTTAGGGTAAAG;His8...
XM_017023671.1:c.3321_*12delinsCTATTCATAAGTTAGGGTAAAG XP_016879160.1:n.[c.3321_*12delinsCTATTCATAAGTTAGGGTAAAG;His1...
XM_017023672.2:c.3315_*12delinsCTATTCATAAGTTAGGGTAAAG XP_016879161.1:n.[c.3315_*12delinsCTATTCATAAGTTAGGGTAAAG;His1...
XM_017023673.2:c.*187_*208delinsCTATTCATAAGTTAGGGTAAAG XP_016879162.1:n.*187_*208delinsCTATTCATAAGTTAGGGTAAAG
NM_024675.4:c.3552_*12delinsCTATTCATAAGTTAGGGTAAAG MANE Select NP_078951.2:n.[c.3552_*12delinsCTATTCATAAGTTAGGGTAAAG;His1184...