Canonical Allele Identifier: CA2213410583
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621604_23621605delinsGA , CM000678.2:g.23621604_23621605delinsGA GRCh38
NC_000016.9:g.23632925_23632926delinsGA , CM000678.1:g.23632925_23632926delinsGA GRCh37
NC_000016.8:g.23540426_23540427delinsGA NCBI36
NG_007406.1:g.24753_24754delinsTC , LRG_308:g.24753_24754delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3003-127_3003-126delinsTC ENSP00000460666.3:n.3003-127_3003-126delinsTC
ENST00000565038.2:c.*478-127_*478-126delinsTC ENSP00000459882.2:n.*478-127_*478-126delinsTC
ENST00000566069.6:c.2997-127_2997-126delinsTC ENSP00000459237.2:n.2997-127_2997-126delinsTC
ENST00000697377.2:c.2841-127_2841-126delinsTC ENSP00000513286.2:n.2841-127_2841-126delinsTC
ENST00000697379.2:c.3003-127_3003-126delinsTC ENSP00000513287.2:n.3003-127_3003-126delinsTC
ENST00000561514.2:c.2112-127_2112-126delinsTC ENSP00000460666.2:n.2112-127_2112-126delinsTC
ENST00000697374.1:c.2112-127_2112-126delinsTC ENSP00000513284.1:n.2112-127_2112-126delinsTC
ENST00000697375.1:n.4344-127_4344-126delinsTC
ENST00000697376.1:c.2112-127_2112-126delinsTC ENSP00000513285.1:n.2112-127_2112-126delinsTC
ENST00000697377.1:c.1950-127_1950-126delinsTC ENSP00000513286.1:n.1950-127_1950-126delinsTC
ENST00000697378.1:n.3517-127_3517-126delinsTC
ENST00000697379.1:c.2112-127_2112-126delinsTC ENSP00000513287.1:n.2112-127_2112-126delinsTC
ENST00000697380.1:n.2289-127_2289-126delinsTC
ENST00000697381.1:n.1692-127_1692-126delinsTC
ENST00000697382.1:c.2112-127_2112-126delinsTC ENSP00000513288.1:n.2112-127_2112-126delinsTC
ENST00000697383.1:c.531-127_531-126delinsTC ENSP00000513289.1:n.531-127_531-126delinsTC
ENST00000261584.9:c.2997-127_2997-126delinsTC MANE Select ENSP00000261584.4:n.2997-127_2997-126delinsTC
ENST00000261584.8:c.2997-127_2997-126delinsTC ENSP00000261584.4:n.2997-127_2997-126delinsTC
ENST00000568219.5:c.2112-127_2112-126delinsTC ENSP00000454703.2:n.2112-127_2112-126delinsTC
NM_024675.3:c.2997-127_2997-126delinsTC , LRG_308t1:c.2997-127_2997-126delinsTC NP_078951.2:n.2997-127_2997-126delinsTC
XM_011545946.1:c.3003-127_3003-126delinsTC XP_011544248.1:n.3003-127_3003-126delinsTC
XM_011545947.1:c.3003-127_3003-126delinsTC XP_011544249.1:n.3003-127_3003-126delinsTC
XM_011545948.1:c.2112-127_2112-126delinsTC XP_011544250.1:n.2112-127_2112-126delinsTC
XR_950851.1:n.3793-127_3793-126delinsTC
XM_011545946.2:c.3003-127_3003-126delinsTC XP_011544248.1:n.3003-127_3003-126delinsTC
XM_011545947.2:c.3003-127_3003-126delinsTC XP_011544249.1:n.3003-127_3003-126delinsTC
XM_011545948.2:c.2112-127_2112-126delinsTC XP_011544250.1:n.2112-127_2112-126delinsTC
XM_017023671.1:c.3003-127_3003-126delinsTC XP_016879160.1:n.3003-127_3003-126delinsTC
XM_017023672.2:c.2997-127_2997-126delinsTC XP_016879161.1:n.2997-127_2997-126delinsTC
XM_017023673.2:c.2997-127_2997-126delinsTC XP_016879162.1:n.2997-127_2997-126delinsTC
NM_024675.4:c.2997-127_2997-126delinsTC MANE Select NP_078951.2:n.2997-127_2997-126delinsTC