Canonical Allele Identifier: CA915949168
Gene: PALB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 648347
dbSNP Id: rs1597079941

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23621474_23621476delinsGT , CM000678.2:g.23621474_23621476delinsGT GRCh38
NC_000016.9:g.23632795_23632797delinsGT , CM000678.1:g.23632795_23632797delinsGT GRCh37
NC_000016.8:g.23540296_23540298delinsGT NCBI36
NG_007406.1:g.24882_24884delinsAC , LRG_308:g.24882_24884delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3005_3007delinsAC ENSP00000460666.3:p.Gly1002AspfsTer7
ENST00000565038.2:c.*480_*482delinsAC ENSP00000459882.2:n.*480_*482delinsAC
ENST00000566069.6:c.2999_3001delinsAC ENSP00000459237.2:p.Gly1000AspfsTer7
ENST00000697377.2:c.2843_2845delinsAC ENSP00000513286.2:p.Gly948AspfsTer7
ENST00000697379.2:c.3005_3007delinsAC ENSP00000513287.2:p.Gly1002AspfsTer7
ENST00000561514.2:c.2114_2116delinsAC ENSP00000460666.2:p.Gly705AspfsTer7
ENST00000697374.1:c.2114_2116delinsAC ENSP00000513284.1:p.Gly705AspfsTer7
ENST00000697375.1:n.4346_4348delinsAC
ENST00000697376.1:c.2114_2116delinsAC ENSP00000513285.1:p.Gly705AspfsTer7
ENST00000697377.1:c.1952_1954delinsAC ENSP00000513286.1:p.Gly651AspfsTer7
ENST00000697378.1:n.3519_3521delinsAC
ENST00000697379.1:c.2114_2116delinsAC ENSP00000513287.1:p.Gly705AspfsTer7
ENST00000697380.1:n.2291_2293delinsAC
ENST00000697381.1:n.1694_1696delinsAC
ENST00000697382.1:c.2114_2116delinsAC ENSP00000513288.1:p.Gly705AspfsTer7
ENST00000697383.1:c.533_535delinsAC ENSP00000513289.1:p.Gly178AspfsTer7
ENST00000261584.9:c.2999_3001delinsAC MANE Select ENSP00000261584.4:p.Gly1000AspfsTer7
ENST00000261584.8:c.2999_3001delinsAC ENSP00000261584.4:p.Gly1000AspfsTer7
ENST00000568219.5:c.2114_2116delinsAC ENSP00000454703.2:p.Gly705AspfsTer7
NM_024675.3:c.2999_3001delinsAC , LRG_308t1:c.2999_3001delinsAC NP_078951.2:p.Gly1000AspfsTer7
XM_011545946.1:c.3005_3007delinsAC XP_011544248.1:p.Gly1002AspfsTer7
XM_011545947.1:c.3005_3007delinsAC XP_011544249.1:p.Gly1002AspfsTer7
XM_011545948.1:c.2114_2116delinsAC XP_011544250.1:p.Gly705AspfsTer7
XR_950851.1:n.3795_3797delinsAC
XM_011545946.2:c.3005_3007delinsAC XP_011544248.1:p.Gly1002AspfsTer7
XM_011545947.2:c.3005_3007delinsAC XP_011544249.1:p.Gly1002AspfsTer7
XM_011545948.2:c.2114_2116delinsAC XP_011544250.1:p.Gly705AspfsTer7
XM_017023671.1:c.3005_3007delinsAC XP_016879160.1:p.Gly1002AspfsTer7
XM_017023672.2:c.2999_3001delinsAC XP_016879161.1:p.Gly1000AspfsTer7
XM_017023673.2:c.2999_3001delinsAC XP_016879162.1:p.Gly1000AspfsTer7
NM_024675.4:c.2999_3001delinsAC MANE Select NP_078951.2:p.Gly1000AspfsTer7