Canonical Allele Identifier: CA164092
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs587776428

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23603515_23603516del , CM000678.2:g.23603515_23603516del GRCh38
NC_000016.9:g.23614836_23614837del , CM000678.1:g.23614836_23614837del GRCh37
NC_000016.8:g.23522337_23522338del NCBI36
NG_007406.1:g.42845_42846del , LRG_308:g.42845_42846del

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.3513_3514del ENSP00000460666.3:p.His1172PhefsTer19
ENST00000565038.2:c.*992_*993del ENSP00000459882.2:n.*992_*993del
ENST00000566069.6:c.*142_*143del ENSP00000459237.2:n.*142_*143del
ENST00000697377.2:c.3351_3352del ENSP00000513286.2:p.His1118PhefsTer19
ENST00000697379.2:c.3513_3514del ENSP00000513287.2:p.His1172PhefsTer19
ENST00000561514.2:c.2622_2623del ENSP00000460666.2:p.His875PhefsTer19
ENST00000697374.1:c.2622_2623del ENSP00000513284.1:p.His875PhefsTer19
ENST00000697375.1:n.4854_4855del
ENST00000697376.1:c.*142_*143del ENSP00000513285.1:n.*142_*143del
ENST00000697377.1:c.2460_2461del ENSP00000513286.1:p.His821PhefsTer19
ENST00000697378.1:n.4027_4028del
ENST00000697379.1:c.2622_2623del ENSP00000513287.1:p.His875PhefsTer19
ENST00000697380.1:n.2711_2712del
ENST00000697381.1:n.2202_2203del
ENST00000697382.1:c.*284_*285del ENSP00000513288.1:n.*284_*285del
ENST00000697383.1:c.1041_1042del ENSP00000513289.1:p.His348PhefsTer19
ENST00000261584.9:c.3507_3508del MANE Select ENSP00000261584.4:p.His1170PhefsTer19
ENST00000261584.8:c.3507_3508del ENSP00000261584.4:p.His1170PhefsTer19
ENST00000566069.5:c.273_274del
ENST00000568219.5:c.2622_2623del ENSP00000454703.2:p.His875PhefsTer19
NM_024675.3:c.3507_3508del , LRG_308t1:c.3507_3508del NP_078951.2:p.His1170PhefsTer19
XM_011545946.1:c.3513_3514del XP_011544248.1:p.His1172PhefsTer19
XM_011545947.1:c.*142_*143del XP_011544249.1:n.*142_*143del
XM_011545948.1:c.2622_2623del XP_011544250.1:p.His875PhefsTer19
XR_950851.1:n.4215_4216del
XM_011545946.2:c.3513_3514del XP_011544248.1:p.His1172PhefsTer19
XM_011545947.2:c.*142_*143del XP_011544249.1:n.*142_*143del
XM_011545948.2:c.2622_2623del XP_011544250.1:p.His875PhefsTer19
XM_017023671.1:c.3276_3277del XP_016879160.1:p.His1093PhefsTer19
XM_017023672.2:c.3270_3271del XP_016879161.1:p.His1091PhefsTer19
XM_017023673.2:c.*142_*143del XP_016879162.1:n.*142_*143del
NM_024675.4:c.3507_3508del MANE Select NP_078951.2:p.His1170PhefsTer19