Canonical Allele Identifier: CA2213407973
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs1966744848

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23619957_23619960del , CM000678.2:g.23619957_23619960del GRCh38
NC_000016.9:g.23631278_23631281del , CM000678.1:g.23631278_23631281del GRCh37
NC_000016.8:g.23538779_23538782del NCBI36
NG_007406.1:g.26398_26401del , LRG_308:g.26398_26401del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3119+1402_3119+1405del ENSP00000460666.3:n.3119+1402_3119+1405del
ENST00000565038.2:c.*594+1402_*594+1405del ENSP00000459882.2:n.*594+1402_*594+1405del
ENST00000566069.6:c.3113+1402_3113+1405del ENSP00000459237.2:n.3113+1402_3113+1405del
ENST00000697377.2:c.2957+1402_2957+1405del ENSP00000513286.2:n.2957+1402_2957+1405del
ENST00000697379.2:c.3119+1402_3119+1405del ENSP00000513287.2:n.3119+1402_3119+1405del
ENST00000561514.2:c.2228+1402_2228+1405del ENSP00000460666.2:n.2228+1402_2228+1405del
ENST00000697374.1:c.2228+1402_2228+1405del ENSP00000513284.1:n.2228+1402_2228+1405del
ENST00000697375.1:n.4460+1402_4460+1405del
ENST00000697376.1:c.2228+1402_2228+1405del ENSP00000513285.1:n.2228+1402_2228+1405del
ENST00000697377.1:c.2066+1402_2066+1405del ENSP00000513286.1:n.2066+1402_2066+1405del
ENST00000697378.1:n.3633+1402_3633+1405del
ENST00000697379.1:c.2228+1402_2228+1405del ENSP00000513287.1:n.2228+1402_2228+1405del
ENST00000697380.1:n.2405+1402_2405+1405del
ENST00000697381.1:n.1808+1402_1808+1405del
ENST00000697382.1:c.2228+1402_2228+1405del ENSP00000513288.1:n.2228+1402_2228+1405del
ENST00000697383.1:c.647+1402_647+1405del ENSP00000513289.1:n.647+1402_647+1405del
ENST00000261584.9:c.3113+1402_3113+1405del MANE Select ENSP00000261584.4:n.3113+1402_3113+1405del
ENST00000261584.8:c.3113+1402_3113+1405del ENSP00000261584.4:n.3113+1402_3113+1405del
ENST00000566069.5:c.28+1402_28+1405del
ENST00000568219.5:c.2228+1402_2228+1405del ENSP00000454703.2:n.2228+1402_2228+1405del
NM_024675.3:c.3113+1402_3113+1405del , LRG_308t1:c.3113+1402_3113+1405del NP_078951.2:n.3113+1402_3113+1405del
XM_011545946.1:c.3119+1402_3119+1405del XP_011544248.1:n.3119+1402_3119+1405del
XM_011545947.1:c.3119+1402_3119+1405del XP_011544249.1:n.3119+1402_3119+1405del
XM_011545948.1:c.2228+1402_2228+1405del XP_011544250.1:n.2228+1402_2228+1405del
XR_950851.1:n.3909+1402_3909+1405del
XM_011545946.2:c.3119+1402_3119+1405del XP_011544248.1:n.3119+1402_3119+1405del
XM_011545947.2:c.3119+1402_3119+1405del XP_011544249.1:n.3119+1402_3119+1405del
XM_011545948.2:c.2228+1402_2228+1405del XP_011544250.1:n.2228+1402_2228+1405del
XM_017023671.1:c.3119+1402_3119+1405del XP_016879160.1:n.3119+1402_3119+1405del
XM_017023672.2:c.3113+1402_3113+1405del XP_016879161.1:n.3113+1402_3113+1405del
XM_017023673.2:c.3113+1402_3113+1405del XP_016879162.1:n.3113+1402_3113+1405del
NM_024675.4:c.3113+1402_3113+1405del MANE Select NP_078951.2:n.3113+1402_3113+1405del