Canonical Allele Identifier: CA719227242
Gene: PALB2 HGNC NCBI

Linked Data

dbSNP Id: rs1320566288

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621301_23621302del , CM000678.2:g.23621301_23621302del GRCh38
NC_000016.9:g.23632622_23632623del , CM000678.1:g.23632622_23632623del GRCh37
NC_000016.8:g.23540123_23540124del NCBI36
NG_007406.1:g.25058_25059del , LRG_308:g.25058_25059del

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3119+62_3119+63del ENSP00000460666.3:n.3119+62_3119+63del
ENST00000565038.2:c.*594+62_*594+63del ENSP00000459882.2:n.*594+62_*594+63del
ENST00000566069.6:c.3113+62_3113+63del ENSP00000459237.2:n.3113+62_3113+63del
ENST00000697377.2:c.2957+62_2957+63del ENSP00000513286.2:n.2957+62_2957+63del
ENST00000697379.2:c.3119+62_3119+63del ENSP00000513287.2:n.3119+62_3119+63del
ENST00000561514.2:c.2228+62_2228+63del ENSP00000460666.2:n.2228+62_2228+63del
ENST00000697374.1:c.2228+62_2228+63del ENSP00000513284.1:n.2228+62_2228+63del
ENST00000697375.1:n.4460+62_4460+63del
ENST00000697376.1:c.2228+62_2228+63del ENSP00000513285.1:n.2228+62_2228+63del
ENST00000697377.1:c.2066+62_2066+63del ENSP00000513286.1:n.2066+62_2066+63del
ENST00000697378.1:n.3633+62_3633+63del
ENST00000697379.1:c.2228+62_2228+63del ENSP00000513287.1:n.2228+62_2228+63del
ENST00000697380.1:n.2405+62_2405+63del
ENST00000697381.1:n.1808+62_1808+63del
ENST00000697382.1:c.2228+62_2228+63del ENSP00000513288.1:n.2228+62_2228+63del
ENST00000697383.1:c.647+62_647+63del ENSP00000513289.1:n.647+62_647+63del
ENST00000261584.9:c.3113+62_3113+63del MANE Select ENSP00000261584.4:n.3113+62_3113+63del
ENST00000261584.8:c.3113+62_3113+63del ENSP00000261584.4:n.3113+62_3113+63del
ENST00000566069.5:c.28+62_28+63del
ENST00000568219.5:c.2228+62_2228+63del ENSP00000454703.2:n.2228+62_2228+63del
NM_024675.3:c.3113+62_3113+63del , LRG_308t1:c.3113+62_3113+63del NP_078951.2:n.3113+62_3113+63del
XM_011545946.1:c.3119+62_3119+63del XP_011544248.1:n.3119+62_3119+63del
XM_011545947.1:c.3119+62_3119+63del XP_011544249.1:n.3119+62_3119+63del
XM_011545948.1:c.2228+62_2228+63del XP_011544250.1:n.2228+62_2228+63del
XR_950851.1:n.3909+62_3909+63del
XM_011545946.2:c.3119+62_3119+63del XP_011544248.1:n.3119+62_3119+63del
XM_011545947.2:c.3119+62_3119+63del XP_011544249.1:n.3119+62_3119+63del
XM_011545948.2:c.2228+62_2228+63del XP_011544250.1:n.2228+62_2228+63del
XM_017023671.1:c.3119+62_3119+63del XP_016879160.1:n.3119+62_3119+63del
XM_017023672.2:c.3113+62_3113+63del XP_016879161.1:n.3113+62_3113+63del
XM_017023673.2:c.3113+62_3113+63del XP_016879162.1:n.3113+62_3113+63del
NM_024675.4:c.3113+62_3113+63del MANE Select NP_078951.2:n.3113+62_3113+63del