Canonical Allele Identifier: CA2695197565
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23638094_23638095del , CM000678.2:g.23638094_23638095del GRCh38
NC_000016.9:g.23649415_23649416del , CM000678.1:g.23649415_23649416del GRCh37
NC_000016.8:g.23556916_23556917del NCBI36
NG_007406.1:g.8264_8265del , LRG_308:g.8264_8265del

Transcript Alleles

HGVS Amino-acid Change
NM_024675.4:c.84_85del MANE Select NP_078951.2:p.Tyr28Ter
ENST00000261584.9:c.84_85del MANE Select ENSP00000261584.4:p.Tyr28Ter
NM_024675.3:c.84_85del , LRG_308t1:c.84_85del NP_078951.2:p.Tyr28Ter
ENST00000261584.8:c.84_85del ENSP00000261584.4:p.Tyr28Ter
ENST00000561514.1:c.90_91del ENSP00000460666.1:p.Tyr30Ter
ENST00000561514.2:c.-802_-801del ENSP00000460666.2:n.-802_-801del
ENST00000561514.3:c.90_91del ENSP00000460666.3:p.Tyr30Ter
ENST00000565038.2:c.84_85del ENSP00000459882.2:p.Tyr28Ter
ENST00000566069.6:c.84_85del ENSP00000459237.2:p.Tyr28Ter
ENST00000567003.1:n.362_363del
ENST00000568219.5:c.-802_-801del ENSP00000454703.2:n.-802_-801del
ENST00000697374.1:c.-802_-801del ENSP00000513284.1:n.-802_-801del
ENST00000697375.1:n.1431_1432del
ENST00000697376.1:c.-838_-837del ENSP00000513285.1:n.-838_-837del
ENST00000697377.1:c.-802_-801del ENSP00000513286.1:n.-802_-801del
ENST00000697377.2:c.90_91del ENSP00000513286.2:p.Tyr30Ter
ENST00000697378.1:n.604_605del
ENST00000697379.1:c.-802_-801del ENSP00000513287.1:n.-802_-801del
ENST00000697379.2:c.90_91del ENSP00000513287.2:p.Tyr30Ter
ENST00000697382.1:c.-802_-801del ENSP00000513288.1:n.-802_-801del
ENST00000697383.1:c.48+3016_48+3017del ENSP00000513289.1:n.48+3016_48+3017del
ENST00000697384.1:n.238_239del
XM_011545946.1:c.90_91del XP_011544248.1:p.Tyr30Ter
XM_011545946.2:c.90_91del XP_011544248.1:p.Tyr30Ter
XM_011545947.1:c.90_91del XP_011544249.1:p.Tyr30Ter
XM_011545947.2:c.90_91del XP_011544249.1:p.Tyr30Ter
XM_011545948.1:c.-802_-801del XP_011544250.1:n.-802_-801del
XM_011545948.2:c.-802_-801del XP_011544250.1:n.-802_-801del
XM_017023671.1:c.90_91del XP_016879160.1:p.Tyr30Ter
XM_017023672.2:c.84_85del XP_016879161.1:p.Tyr28Ter
XM_017023673.2:c.84_85del XP_016879162.1:p.Tyr28Ter
XR_950851.1:n.880_881del