Canonical Allele Identifier: CA2213436421
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23641118_23641121delinsTCTC , CM000678.2:g.23641118_23641121delinsTCTC GRCh38
NC_000016.9:g.23652439_23652442delinsTCTC , CM000678.1:g.23652439_23652442delinsTCTC GRCh37
NC_000016.8:g.23559940_23559943delinsTCTC NCBI36
NG_007406.1:g.5237_5240delinsGAGA , LRG_308:g.5237_5240delinsGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.-816_-813delinsGAGA ENSP00000460666.3:n.-816_-813delinsGAGA
ENST00000565038.2:c.37_40delinsGAGA ENSP00000459882.2:p.Glu13=
ENST00000566069.6:c.37_40delinsGAGA ENSP00000459237.2:p.Glu13=
ENST00000697377.2:c.-203_-200delinsGAGA ENSP00000513286.2:n.-203_-200delinsGAGA
ENST00000697379.2:c.-109_-106delinsGAGA ENSP00000513287.2:n.-109_-106delinsGAGA
ENST00000561514.2:c.-1707_-1704delinsGAGA ENSP00000460666.2:n.-1707_-1704delinsGAGA
ENST00000697374.1:c.-1298_-1295delinsGAGA ENSP00000513284.1:n.-1298_-1295delinsGAGA
ENST00000697376.1:c.-1019_-1016delinsGAGA ENSP00000513285.1:n.-1019_-1016delinsGAGA
ENST00000697377.1:c.-1094_-1091delinsGAGA ENSP00000513286.1:n.-1094_-1091delinsGAGA
ENST00000697379.1:c.-1000_-997delinsGAGA ENSP00000513287.1:n.-1000_-997delinsGAGA
ENST00000697382.1:c.-1758_-1755delinsGAGA ENSP00000513288.1:n.-1758_-1755delinsGAGA
ENST00000697383.1:c.37_40delinsGAGA ENSP00000513289.1:p.Glu13=
ENST00000697384.1:n.191_194delinsGAGA
ENST00000261584.9:c.37_40delinsGAGA MANE Select ENSP00000261584.4:p.Glu13=
ENST00000261584.8:c.37_40delinsGAGA ENSP00000261584.4:p.Glu13=
ENST00000567003.1:n.181_184delinsGAGA
ENST00000568219.5:c.-838+6_-838+9delinsGAGA ENSP00000454703.2:n.-838+6_-838+9delinsGAGA
NM_024675.3:c.37_40delinsGAGA , LRG_308t1:c.37_40delinsGAGA NP_078951.2:p.Glu13=
XM_011545948.1:c.-983_-980delinsGAGA XP_011544250.1:n.-983_-980delinsGAGA
XM_011545946.2:c.-816_-813delinsGAGA XP_011544248.1:n.-816_-813delinsGAGA
XM_011545947.2:c.-816_-813delinsGAGA XP_011544249.1:n.-816_-813delinsGAGA
XM_011545948.2:c.-983_-980delinsGAGA XP_011544250.1:n.-983_-980delinsGAGA
XM_017023671.1:c.-816_-813delinsGAGA XP_016879160.1:n.-816_-813delinsGAGA
XM_017023672.2:c.37_40delinsGAGA XP_016879161.1:p.Glu13=
XM_017023673.2:c.37_40delinsGAGA XP_016879162.1:p.Glu13=
NM_024675.4:c.37_40delinsGAGA MANE Select NP_078951.2:p.Glu13=